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1996-1997 Research Agenda - Request for Applications

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Length: 36 pages
800105375-800106143
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Named Organization
World Health Organization
University of Minnesota
University of Lisbon
NYU Medical Center
Concordia University
University of Vermont
Colorado State University
University of Pittsburgh
University of Gothenburg
San Diego State University
University of Missouri-Rolla
University of Tulsa
Wake Forest University
University of Toledo
Tufts University
US Public Health Service
National Institute of Standards and Technology
Virginia Commonwealth University
US FDA
University of Washington
University of Illinois
Philip Morris USA
Brown & Williamson Tobacco Corporation
Japan Tobacco Incorporated
US EPA
Meharry Medical College
Oak Ridge National Laboratory
US Department of Energy
TRC Environmental Corporation
Washington University
Campbell University
Danish National Institute of Occupational Health
Penn State University
Science Advisory Board
Svenska Tobaks AB
Ecusta
Texas A&M University
Meckler Engineers Group
University of Arkansas for Medical Sciences
University of Aarhus
Proctor & Gamble
Ford Motor Company
Virginia Polytechnic Institute
NIEHS
Standard Commercial Corporation
Shorewood Packaging
Pennsylvania State University, The
University of Mysore
University of Tennessee, The
DIMON International
Cornell University Medical Centre
New York University Medical Centre
Ottawa
Mead Paper
Mundet International Limited
Quest International Flavors USA
Somerville Packaging Corporation
United Technologies Carrier Corporation
Gas Research Institute
Touro College
United Technologies Research Centre
ITRI
University of Alaska Fairbanks
Dorgan Associates
NYU Medical Centre
ICF Kaiser Engineers Incorporated
National Medical Advisory Service Incorporated
University of North Arizona
Synesthetics Incorporated
Apex Environmental Incorporated
Tulane University Medical Centre
Rexair Incorporated
Battelle
St Louis University
Building Science Corporation
IRC Canada
University of Denvar
Johnston Controls Incorporated
National Centre for Occupational Health South Africa
Prairie Swine Centre Incorporated
Health Effects Institute, The
University of Kentucky
University of California
University of Texas
University of Reading
Southern Illinois University
RJ Reynolds Tobacco GmbH
University of Maryland
Johns Hopkins School of Hygiene and Public Health
Illinois Institute of Technology
Brookhaven National Laboratory
Virginia Polytechnic Institute and State University
Universal Corporation
Lorillard Corporation
Utah State University
American Health Foundation
Harvard School of Public Health
University of Wisconsin Hospital
Ohio State University
University of Maryland School of Medicine
Boston University School of Public Health
Jacksonville University
National Institute of Health Guidelines Committee
Northeastern University
University of North Carolina
Named Person
Lebowitz, Michael D
Woods, James E
Levetin, Estelle
Eisenberg, Max
Kessler, Irving
Matanoski, Genevieve M
Utell, Mark J
Wolf, Alfred P
Adams, Eric W
Arora, Sanjay
Aust, Steven D
Bascom, Rebecca
Bell, Iris R
Benjaminson, MA
Billick, Irwin H
Blumenthal, Malcolm N
Brennan, Terry
Burleson, Gary R
Burrell, Robert
Cheek, Jeffrey
Chen, Qingyan
Croome, Derek J
Crouse, William E
Cain, William S
Das, Salil K
Delumyea, R Del
Dorgan, Charles
Dowell, Russell T
Driscoll, Kevin
Dunn, Bonnie
Evans, Hugh L
Fales, Henry M
Frampton, Mark W
Larson, Susan M
Francis, Bettina M
Gardner, Donald
Last, Jerold A
Gearhart, Jeffrey
Getchell, Thomas V
Giardino, Nicholas J
Giese, Roger
Gilbert, Stephen L
Hedge, Alan
Lehrer, Samuel B
Glicksman, Leon R
Ford, Timothy
Jenkins, Roger A
Gong, Henry
Meckler, Milton
Gordon, Terry
Greene, Robert
Haghighat, Fariborz
Hajjar, David
Hasselblad, Victor
Hemenway, David
Reif, John
Roboz, John
Rogers, John M
Sen, Mihir
Sharma, Vinod Kumar
Silver, Wayne
Smith, Douglas A
Stoner, Gary D
Stuart, Bruce
Temple, Robert W
Turner, Simon
Tyler, Walter S
Ultman, James
Wallace, Lance
Wispe, John
Yager, James
Yang, Chin S
Zhang, Yuanhui
Guerin, Michael R
Lewis, Roger
Lippman, Morton
Witschi, Hanspeter
Kilpatrick, James
Akland, Gerald
Burge, Harriet
Bush, Robert
Djordjevic, Mirjana
Dockery, Douglas W
Doty, Richard L
Hoidal, John R
Johnting, Jennifer
Kanarek, Marty S
Kleeberger, Steven R
Kleinman, Michael T
Knutson, Earl
Kuhlman, Michael R
Lewis, Robert
Loyalka, Sudarshan K
McGrath, James J
Mennear, John H
Nielson, Gunnar
Ogden, Michael
Otto, David
Rohde, Charles
Spannhake, E William
Valberg, Peter
Moschandreas, Demetrios
Arey, Janet
Hoffman, Dietrich
Bohanon, Hoy
Nagda, Niren L
Brunnemann, Klaus
Kilpatrick, S James
Camboni, Silvana
Klinger, Lorry A
Menzel, Daniel
Palmer, Kenneth C
Potter, William T
Ramsey, J Michael
Stedman, Donald H
Benson, Janet
Baker, AJ
Castagnoli, Neal
Costa, Daniel L
Rood, Mark J
Lacey, John
Leith, David
Bement, Collette L
Boyse, William K
Christianson, Leslie L
Cosma, Greg
Costa, Lucio G
Cunningham, Jennifer B
Dharamsi, Amin
Duffy, Lawrence K
Eastmond, David A
Fang, Jin Bao
Gatley, John
Gilbert, Avery Nelson
Gilmour, Matthew Ian
Gornes, Joao FP
Goud, S Niranjan
Graham, Charles W
Grinsh, Sergey A
Hittle, Doug C
Holbrook, G Thomas
Horner, W Elliott
Hung, Ling-Ling
Inyang, Hilary I
Keller, John G
Kjaergaard, Soren
Koch, Wendy H
Lehnert, Bruce
Linn, Bill
Lorig, Tyler S
Madhusudhan, B
Koller, Loren
Koutrakis, Petros
Nishimoto, Marc
O'Callaghan, Michael W
O'Neil, Carol
Otten, James
Ritter, Gary L
Saman, Namir
Samini, Behzad S
Ryan, Lisa
Smith, Raymond A
Sauer, Hary J
Sawnor, Marcia
Solornon, Jerome J
Swift, David L
van Berkel, Gary
Yousefi, Vali
Zannetti, Paolo
Zelikoff, Judiath T
Notes

Author name is not available in the document Missing originals: 800105409-800106141. Handwritten.

UCSF Code
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Type
agenda
table
Region
United Kingdom
China
Sweden
Canada
South Africa
Date Loaded
01 Dec 2004
Box
0161
Folder
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-t • CENTER FOR INDOOR AIR RESEARCH 1996-t997 RESEARCH AGENDA REQUEST FOR APPLICATIONS 0 0 BATCo US DOJ v Philip Morris
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Mission Statement The mission of the Center for Indoor Air Research is to sponsor high quality research on indoor air issues and to facilitate communication of research findings to the broad .scientific community. Science Advisory Board Members William S. Cain, Ph.D. Professor, Department of Surgery (Otolaryngology) University of Califomia, San Diego Michael R. Guerin, Ph.D. Head, Organic Chemistry Section Analytical Chemistry Division Oak Ridge National Laboratory Irving Kessler, M.D., Dr.P.H. Professor, Department of Epidemiology and Preventive Medicine University of Maryland School of Medicine Morton Lippmann, Ph.D. Vice-Chairman, Department of Environmental Medicine New York University Medical Center Genevieve M. MatanOski, M.D., Dr.P.H. Professor, Department of Epidemiology Johns Hopkins School of Hygiene and Public Health Demelrios Moschandreas, Ph.D. Professor, Pritzker Department of Environmental Engineering Illinois Institute of Technology Mark J. Utell, M.D. Professor, Medicine and Toxicology University of Rochester School of Medicine Alfred P. Wolf, Ph.D. Director, Cyclotron - PET Program Brookhaven National Laboratory James E. Woods, Jr., Ph.D., P.E. Professor, College of Architecture and Urban Studies Virginia Polytechnic Institute and State University t3ATCo US DOJ v Philip Morris
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J~uary, 1996 Dear Investigator: I am plsased to provide you th~ Center for Indoor Air Research's "Request for Applications" booklet. This package includes information about the Center, the research and review process, procedures for application, the contract man- agement process and the application forms. Also included is our Research Agenda which describes CIAR's research interests. Applications must be postmarked by June 1st. Funding of awarded projects begins the following January I st. If you have additional questions concerning application procedures, please contact the Center at (410) 684-3777, Thank you for your interest. Sincerely, "°" J Bg~Co US DO
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Table of Contents Research and Review Process .................................................................................. 3 Research Agenda .................................................................................................... ... 5 Application Process ................................................................................................. 10 Management of Research Contracts ....................................................................... 10 Contract Administration Policy .............................................................................. 11 Application - General Information and Instructions ............................................. 12 Application Forms .......................................................................................... FI - F3 Appendix A: CIAR Membership ........................................................................... 15 Appendix B: CIAR Peer Reviewers ....................................................................... 17 Appendix C: CIAR Final Report Guidelines ......................................................... 25 Acknowledgements ................................................................................................. 26 O0 0 0 0 BATCo US DOJ v Philip Morris
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Center for Indoor Air Research The Center for Indoor Air Research (CIAR) is a non-profit corporation fonmed in March, 1988 to sponsor high quality research on indoor air issues and to facilitate communication of research findings to the broad scien- tific community. The Center has three classes of mem- bership: charter members, regular members and associate members (See Appendix A). The charter members are those corporations that established the Center and are currently providing the majority of the funding. Regular and associate members are those per- sons or corporations that are interested in indoor air quality research but were not involved in the establishment of the Center. The regular members are represented on the Board of Directors while the associate members are not. The Center is actively seeking addi- tional members in both the regular and associate categories. Additional information on membership can be obtained by contacting the Center. The Center has established a Science Advisory Board (SAB) which develops the research agenda for approval by the Board of Directors. The SAB recommends proposals for funding after they have been peer reviewed by the Center's pool of peer reviewers. This structure ensures that only high quality research which will contribute to the knowledge bank on indoor air is recommended for funding. Research and Review Process The research agenda of the Center for Indoor Air Research is formulated by the Science Advisory Board (SAB), a multi-disciplinary group of individuals with reputations for expertise and scientific leadership in the disciplines relevant to indoor air research. The SAB seeks the best judgments of active research scientists as to what scientific information is missing in the various disciplines before independently ascertaining the research priorities of the Center. After the SAB establishes the research agenda, the Center announces to the scientific community at large that research applications in response to the agenda are being accepted. The review of proposals and their selection for funding is accomplished in a scientifically rigorous and objective manner. Applications are reviewed f~t for scientific quality by the appli- cant's peers selected from the group listed in Appendix B. The SAB, in turn, reviews the applications and peer evaluations, and develops recom- mendations on the selection of applications. Studies recommended by the SAB are subject to final approval by the Board of Directors. A staff scientist is assigned to each funded project to monitor the investi- gator's progress and to provide assis- tance to the investigators toward the successful completion of the project. When a project is completed, the investigator submits a draft final report which is reviewed by the Center for its scientific quality and soundness of conclusions. The investigator is encouraged to publish the work in an independent, peer reviewed journal for the benefit of the scientific commtmity at large. ]3ATCo US DOJ v Philip Morris
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Request for Research Applications Introduction The Center for Indoor Air Research was established in 1988, as an inde- pendent, non-profit corporation. Its primary purpose is to sponsor scientific and technical research on the sources, transformation and fate of constituents affecting indoor air quality; on factors governing human exposure to, and retention of those constituents; on the effects of those constituents on health, including exposure-response relation- ships; and on methods of preventing or abating the concentrations of indoor air contaminants. The research program will be supplemented by periodic conference workshops and commissioned monographs. A Science Advisory Board has been assembled to assist in the formation and review of the research program. The Advisory Board consists of eminent scientists from a range of disciplines, including environmental engineering and monitoring, chemistry, toxicology, microbiology, epidemiolo~, behavioral sciences and biostatistics. The following research agenda was established at a Center for Indoor Air Research Science Advisory Board (SAB) Workshop. Research topics of major interest to the Center are described in the agenda. Individuals who intend to apply for funding are encouraged first to submit a letter of intent, two-to-three pages in length, indicating the research objectives, key elements of the experimental design and methods, estimated time required and approximate direct and indirect cost. The letter should be addressed to: Center for Indoor Air Research 1099 Winterson Road, Suite 280 Linthicum, Maryland 21090 | I II O0 0 0 0 0 13ATCo US DOJ v Philip Morns
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Research Agenda In the research agenda that follows, the Center's priorities and specific requests for application are presented. These represent the Center's best judgment on currently important research problems, but the agenda is by no means exhaustive. As stated in the Introduction, any proposal that is consistent with the Center's purpose will be considered. Our objective in presenting priorities and research topics is to stimulate researchers to focus on problems related to indoor air quality (IAQ). The research needs that follow are grouped according to sources investi- gations, exposure/dose assessment, heallh effects, perception of IAQ, and engineering control strategies for IAQ. This collection of topics represents one general approach to indoor air quality research. Numerous indoor air contaminants warrant investigation in terms of their fate and transport in the indoor environment, the forms and quantities in which they present themselves to exposed indi- viduals, the dose actually delivered to a target (e.g., individual, organ, cell), strategies to reduce their levels, and the perception of indoor air quality in the presence and absence of the contam- inants. Some contam.inants of interest are volatile organic compounds (VOCs), environmental tobacco smoke (ETS), biological aerosols (aeroallergens and aeropathogens), and particulate matter. Indoor air quality is "'the nature of air that affects the health and well-being of occupants" where, according to the World Health Organization, "health is a state of complete physical, mental and social well-being, and not merely the absence of disease or infirmity". CIAR is interested in all relevant chemistry, physics, control strategies for, health effects caused or aggravated by, and psychosocial factors influencing the perception of indoor air quality. Due to the interdisciplinary nature of indoor air research, most projects will encompass more than one of these areas. CIAR, therefore, encourages interdepartmental collaborations and joint projects whenever they serve to enhance the interpretation and evalua- tion of results or to strengthen the validity of conclusions. SOUrces Myriad substances in indoor air have potential to affect health. The sources are many (e.g., outdoor air, people and their activities such as cooking, con- sumer products including pesticides, heating and cooling systems, building materials, electronic equipment) and distributions of sources and chemicals vary among indoor environments. For example, certain chemicals might be added to heating/cooling systems to exert a biocidal or preservative effect. The fate and effects of such known- source agents have not been studied extensively. Many constituents are being studied within risk assessment frameworks as toxicologically-signifi- cant compounds; however, much work remains to be done in characterizing distributions of various agents in specific envinmmeats related to sources and assessing their impact on human health. 0 0 0 BATCo US DOJ v Philip Morri,,
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CIAR is interested in creative proposals • Develop methods to characterize and quantify source emissions. Research in this area could include biologically-based means of source characterization and product screening, such as human irritation and odor assays, as well as development/ improvement of chemical analytical methods. • Investigate the transport and environmental fate of indoor air contaminants, particularly via sinks. This work will elucidate indoor air chemistry, and is important in deter- mining concentrations for short and long-term exposure estimates. • Develop and validate models to relate source emissions, fate, and transport. The air in virtually all indoor environ- ments is a complex mixture of low levels of both reactive and unreactive species which may interact chemically or physically in a dynamic equilibrium between gaseous and particulate phas- es. The physical and chemical natures of the species themselves as well as those of the surrounding environment could affect the composition of the air to which an occupant is exposed. For example, does the presence of moisture lead to chemical reactions with indoor air constituents? How and to what extent do different types of building materials and surfaces influence the fate of indoor contaminants? • Elucidate the dynamics of complex physico- chemical mixtures typical of indoor environments. Numerous biological agents in indoor air may cause human disease. The most common biological agents found uo~im~.ry in indoor environments are bacteria, viruses, fungal spores, algae, arthropod fragments and droppings,, and animal dander. Proliferation of microorganisms is dependent on moisture level and temperature. These requirements for growth are often provided by heating and air conditioning systems, and humidifiers. Exposure Assessment/ The estimates of exposure and inter- nal dose are critical factors in the reliability of studies to determine the health consequences of exposures. There are at least two critical issues in exposure-dose relationships: the effect of aerodynamic respiratory tract defenses in altering the quantity and distribution of the exposure to achieve a tissue dose, and measure- ment of actual internal dose. The complex particle-gas composition of indoor air contaminants has an important effect on the pulmonary distribution of the inhaled exposure. Research proposals are requested on the following: • Develop sampling methods amenable to standardization for the characteri- zation of microorganism concentra- tions in the indoor environment. • Characterize the size-segregated distribution of specific antigens in various indoor environmems. Attention should be paid to factors influencing the distribution of the antigen in settled dust and as air- borne particles. Measurements from site-specific and personal monitoring including biomarker measurements, are more reliable than self-reported history of exposure. In epidemiological studies, inaccurate reports of exposure history introduce misclassification bias. In field studies, the use of inaccurate ~0 0 0 0 BATCo US DOJ v Philip Morris
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estimates of exposure can lead to variable, unreliable dose-response data. Appropriate modeling may esti- mate dose from exposure. Biomarkers can be useful in studying tissue injury and to determine dose from the low levels of exposure common indoors. Applications are requested for the following: • Clarify the relationship between experimental measures of exposure and self-reporting as a measure of exposure. • Clarify the relationship between exposure and dosimetry by conducting studies to improve the use of bio- markers together with exposure monitoring and health effects. This effort would involve improvements in pharmacokinetic modeling as well as methods development for exposure research. Particular areas in which there are limited data are: - personal monitoring in non-indus- trial occupations and in high risk groups; - time-activity profiles in exposure studies. • Develop unique, new biomarkers with the sensitivity and specificity to be useful in studying injury in both animals and humans. • Develop assays for detection of biological markers for exposure, effect, and susceptibility. • Investigate the use of polyclonal antibodies for screening in exposure- dose studies. • Develop and validate models to pre- dict dose and allow for extrapolation between animals and humans. Health Effects/Responses Low levels of airborne species may mediate lung injury by effects related to cumulative dose or long-term dose rather than peak dose. This concept is well-established for lead, where total dose is as important as dose pattern. Although there is growing agreement regarding the techniques used to measure indoor contaminants, there remains the problem of whether point or time-weighted measures are most meaningful. Given a specific indoor environment with a characterizable distribution of airborne substances, do measure,able health effects relate to cumulative, chronic, low-level concentrations, to acute peak concen- trations, and/or to synergistic effects between substances? CIAR is interested in considering creative proposals to: • Investigate the effects of long-term steady exposures to non-peak or low levels of indoor contaminants in order to determine whether or not realistic indoor levels of these chem- icals contribute to overall adverse health effects. While many chemical constituents have been identified in indoor air, little is known about the chemical changes that occur therein and the mechanisms by which they occur. The chemical fate of single species and their resulting impacts on health could vary greatly in different complex environments. For example, does the presence of an airborne contaminant or reaction intermediate alter the O 130 13ATCo US DOJ v Philip Morris
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tissue dose and physiological responses to other indoor air contaminants? CIAR will consider creative proposals tO: • Elucidate the health responses of interactive, low-level, complex exposures. Studies of the relationship between indoor air contaminants and precisely def'med cl~cal cl~ases are en~uraged. Health effect/response questions of interest to CIAR include: • Do inhaled indoor contaminants - impair cardiovascular performance and contribute to the incidence of angina and myocardial infarction? - initiate or aggravate bronchial hyperreactivity in asthmatics and/or the normal population? - affect resistance to respiratory infec- tion? - affect prenatal and perinatal development? - affect cognitive performance? CIAR requests applications to: • Perform studies to determine the effects of indoor contaminants on cardiovascular, pulmonary, immune system and behavioral function. • Investigate host susceptibility factors for effects due to inhalation of indoor contaminants. CIAR is interested particularly in the long-term consequences of low level exposures. Biological agents may cause allergenic or pathogenic responses. Indoor allergens, including those present in animal dander and arthropod fragments and droppings, appear to be ubiquitous. Virtually all homes studied, whether or not pets have been present, have exhibited allergens. Such allergens are risk factors in both the development of asthma and provocation of acute asthmatic attacks. Avoidance of the allergens has been associated with improvement in the clinical status of asthma. The extent to which the risk imposed by specific allergens is determined by their aerodynamic characteristics and airborne concen- trations is uncertain. A variety of microorganisms including fungi, bacteria, nematodes and amoebae have been implicated as producers of sensitizing antigens responsible for the development of acute and chronic forms of immunologically mediated disease. Elevated humidity and moist surfaces promote the growth of the parent organisms. The role of aempathogens in inducing allergenic rather than pathogenic responses is an area of interest to the Center. • Conduct highly-focused studies of aempathogens (endogenous bacterial and fungal flora found in specific envimrar~nts which induce allergenic rather than pathogenic responses. Proposed studies in this area should be promising with respect to yielding productive, new results. • Relate such health responses to indicators of host susceptibility. • Develop immunological and biochemical markers that best char- acterize susceptibility and response. Perception of IAQ A basic objective of environmental control is to provide for the comfort and health of occupants. Investigators have not always been able to identify specific contaminants responsible for reported health complaints, the most O0 0 0 0 BATCo US DOJ v Philip Morris
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prevalent being eye, nose, and throat irritation. While considerable progress has been made in the development of technology to measure contaminant concentrations, greater effort is needed in quantifying human responses to indoor air environments. Studies to date have shown that worker health in office buildings, for example, is influenced by individual, perceptual, psychosocial, and psychophysical factors. CIAR requests applications for research to: • Elucidate the relationship among disorders expressed by occupants in buildings and the importance of perception. Determine the baseline rates of symptom reporting under various, well-documented circum- stances. This research would most likely involve the development of improved sampling strategies fog surveying building occupants and improved serf-reporting measures, interview techniques, and o~her approaches to assess occupants' health problems. • Develop convenient, objective ways, based on physiological or biochemical measurements, to assess irritation and to validate symptoms of irrita- tion. Improve the sensitivity of existing indices of eye, throat, and nasal irritation. • Explore the basis for individual and group differences in perceptual sensitivity and annoyance to indoor contaminants. Relevant factors could include age, sex, and personal history of smoking behavior, allergy, and respiratory infection. • Develop and validate a predictive human structure-activity model for irritants. Explore the potential for extrapolating the existing structure- activity data for irritants in animals to humans. • Develop convenient, objective ways based on objective measurements, to assess the impomance of pollutant per- ception on alterations in performance. Engineering Control of IAQ The decrease of indoor contaminants most probably will lead to reduction of adverse health effects. The choice of an engineering control strategy depends strongly on the psychosocial and psychophysical influences described above as well as the measurable environmental contaminant concentrations. Therefore, develop- ment of "healthy building characteris- tics" involves knowledge of both the physical environment and occupant responses. Applications are requested for:. • Developing engineering strategies to control either indoor comfort para- meters or indoor air quality parame- ters, or both. Strategies that enhance the welfare of occupants (comfort parameters) and their health (indoor air parameters) are preferred to controls that address just one or the other. • Developing engineering control strategies to reduce occupant expo- sures to indoor air contaminants in office buildings and in residences. Develop protocols to assess the efficiency of each proposed strategy. • Developing criteria and standards for the design of spaces to be occupied and for design of control systems, to minimize or mitigate indoor air quality problems. O'! BATCo US DOJ v Philip Morris
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Application Process LETTER OF INTENT: CIAR requests submission of a two to three page letter of intent, including a synopsis of the proposed research with reference to the project's specific goal(s), the general approach to be used, identification of all participating institutions and an estimate of the total monies that will be requested. These letters will be used to plan the proposal review process. The letter of intent is not binding on CIAR or the applicant. This letter should be -eceived no later than thirty (30) days prior to the deadline for submitting applications, at the following address: Center for Indoor Air Research 1099 Winterson Road, Suite 280 Linthicum, Maryland 21090 CIAR will notify the applicant ifa full application is not warranted. FORMAT: Applications must be submitted on the attached "Application for CIAR Research Contract". Investigators should review the Application for CIAR Research Contract General Information and Instructions found on pages 12 to 14. Inquiries regarding application procedures and review procedures may be directed to the Center at the above address or by calling (410) 684- 3777. If two appli- cations are interdependent or closely related, they should be appropriately cross-referenced in the project plan. Two copies of the abstract and twelve (original and eleven) copies of the application (including abstracO are needed by CIAR for the review process. Each copy of the application, except the original, should be bound wilh a label containing the title of the proposal and the principal investi- gator's name. DEADLINES: Applications must be postmarked by June 1. Proposals not meeting this deadline will be held for the next funding cycle. Management of Research Contracts Research Agreements The Center for Indoor Air Research awards contracts, renewable annually for the number of years approved by the Board of Directors if work is progressing satisfactorily. The Research Contract has been designed to maximize the integrity of the scien- tific process while providing needed protections and meeting applicable regulations. Proposals and any addenda or modifications will be appended and made part of the contract. Progress Reports Investigators are required to submit progress reports at five months and ten months of each contract year, except for the last year of the project, when the final report is substituted for the usual ten-month report. These reports are reviewed by the project monitor. The basic objective of the five month report is to indicate how much progress has been made in the devel- opment of experimental procedures, which objectives have been completed, and what problems, if any, have arisen. t~ 135 BATCo US DOJ v Philip Morris
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The ten-month report is actually a combined progress report and renewal application for the next year's funding. CIAR's decision regarding renewal of the contract is based upon the informa- tion provided by the investigator in this repo~ The ten-month report should provide a detailed account of experimental results obtained during the funding period, as well as a discus- sion of specific objectives for the coming year and a budget. Site Visits CIAR staff (project monitor) usually conducts site visits to the laboratories of its funded investigators during the project period. The purpose of these visits is to evaluate the status of the project, and to provide an opportunity for an exchange of ideas between the investigator and CIAR scientists. Final Report As part of the research project, the investigator prepares a final report which describes the study and its findings. The investigator's draft final report is reviewed by the project monitor. Some reports are reviewed also by peers who represent a broad range of relevant experience. The objective of the CIAR review process is to ensure that the Investigator's Report is complete, precise, and understandable. Review comments may be sent to the investigator who then has an opportunity to respond to the comments and, if necessary, to revise the report. Guidelines for the preparation of final reports to CIAR appear in Appendix C. Publications It is the policy of the Center to strongly encourage investigators to publish results of research conducted with CIAR funds in the open scientific literature. The following statement, acknowledging CIAR support, should appear in all publications resulting from work funded by CIAR: "Research described in this article was supported (in part) by the Center for Indoor Air Research." Original reprints of all journal articles, copies of abstracts, and review articles describing CIAR-funded research should be sent to the Center. Contract Administration Policy Payments will be made quarterly to the institution where the research is being conducted. A payment schedule other than quarterly must be requested and approved by the Center prior to commencement of a contract. Payments are made upon receipt of an invoice from the institution. It is the Center's policy to permit quarterly billing of 22.5% of the total contract less equipment. Ten percent of the total contract amount is with- held pending receipt and acceptance of the ten-month/final report by the Center. Equipment should be invoiced in the quarter in which it is purchased. Contracts may not be transferred from one institution to another due to a change in affiliation by principal investigator without express permis- sion of the Center. C~ O'1 BATCo US DOJ v Philip Morris
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A Contract may be terminated prior to normal expiration date by the contrac- tor upon notification to the Center with a statement of reasons for termination. Unexpended funds shall be returned to the Center for Indoor Air Research either upon expiration or termination of the project. Budgets are presumed accurate at the time of award; however, up to 20% of the funds may be reapportioned among all categories, except for travel, without prior approval. If, for any unforseen reasons, additional funds or reapportionments exceeding 20% are required, such requests will be consid- ered by the Center upon receipt of a complete statement of reasons for such change. PLEASE NOTE: If funds are reapportioned into category (g), equipment, and/or category(f), sub-contracts, subsequent reduction in category (i), indirect costs, will result and, thus, reduction in the total project award. Application for CIAR Research Contract General Information and Instructions Submission of Applications Complete applications received by the June 1 st postmark deadline will be reviewed. Funding of awarded projects will begin the following January Ist. Submit the original and eleven addi- tional copies. If photographs are included, send one original set. Submit two additional copies of the Research Abstract form. Append as much material as required. Type, single space, using 8 1/2" x 11" paper and label each sheet with the name of the Principal Investigator in the upper right hand comer. Number each page consecutively beginning with page 4. DO NOT insert pages between form pages FI and F3. Investigators will receive written acknowledgement of receipt of the application. Research Plan 8. Aims State the objectives of the research and the hypotheses you will test. 9. Significance of Proposed Work Identify gaps in the research area and discuss pertinent background material that supports the impor- tance of the work. 10. Preliminary Studies Critically evaluate existing knowl- edge pertinent to the application with reference to the key litera- ture. Provide an account of the principal investigator/program director's preliminary studies pertinent to the application and/or any other information that will help to establish the experience and competence of the investigator to pursue the proposed project. 11. Experimental Design and Methods Outline the experimental design and the procedures to be used to accomplish the specific aims of the project. Include the means by O0 0 0 BATCo US DOJ v Philip Morris
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which the data will be collected, analyzed, and interpreted. Include a description of the statistical methods to be used for analysis and interpretation of the data. Describe the proposed statistical procedures with sufficient detail to allow evaluation by a biostadstical reviewer. Describe any new methodology and its advantage over existing methodologies. Discuss the potential difficulties and limitations of the proposed procedures and alternative approaches to achieve the aims. Provide a tentative sequence or timetable for the investigation (i.e., a columnar or graphical represen- tation of your schedule for comple- tion of tasks). Point out any proce- dures, situations, or materials that may be hazardous to personnel and the precautions to be exercised. Provide a list of literature you cited in your application~ 12. Other Support List all currently active and pend- ing support for all key personnel involved in this proposal. Include the source of support, percentage of appointment, dates of project period, a brief description of the project and whether it overlaps, duplicates, replaces, or supplements this proposed work in any way. 13. Budget Cost Data: Provide sufficient detail and analysis to assure the Center that the proposed costs are reasonable and that adequate accounting procedures will be used. CIAR has no specific limita- tion on the budgets of research proposals. Most contracts are expected to be in the range of $50,000 to $200,000 per year, including overhead. Projects requiring larger budgets must have exceptional promise for developing important methods or information for understanding indoor air quality. Personnel: List the names and positions of all applicant organiza- tion personnel involved in the project for which salaries are requested. Note those which are considered essential to the project. Estimate the percentage of time or effort on the project for profes- sional personnel and non-profes- sional personnel. List the dollar amounts separately for each indi- vidual for salary and fringe bene- fits. Fringe benefits may be requested to the extertt that they are treated consistendy by the applying organization as a direct cost to all sponsors. Consultant Costs: Consultant service should be explained by indicating the specific area in which such service is to be used. Identify the contemplated consul- tants. State the number of days of such services estimated to be required and the consultant's quomd rate per day. Equipment: If special-purpose equipment is being proposed, provide a description of the item(s) and details of the proposed cost. If fabrication by the applicant is contemplated, include details of material, labor, and overhead. Alterations and Renovations: If the costs of essential alterations of facilities, including repairs, paint- ing, removal or installation of par- titions, shielding, or air condition- ing, are requested, itemize them by category and justify them fully. BATCo US DOJ v Philip Morris
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Supplies and Other Expenses: All supplies and other expenses should be itemized in sufficient detail to allow reviewers to understand the major categories of expenditures (i.e., animals, glassware, media chemicals, as well as publication costs, page charges, and books, listed by category and unit cost). Itemize and justify such items as patient travel and per diem costs, rentals, leases, and computer costs. Unusually expensive items for spe- cial processes should be separately identified by quantity and price and the use or application thoroughly explained in the project plan. Each individual expense item must be categorized as supplies or other expenses according to the practices of the accounting office of your institution. Travel Expenses: Indicate the esti- mated number of trips required, destination, reason for travel, and cost. Identify and support any other special transportation costs attributable to the performance of this project. CIAR ?ays for foreign travel only if it is approved in advance of the trip. Subcontracts: Itemize and enter a total for these costs. Describe and justify all appropriate costs for ser- vices purchased for, or associated with, third parties. Indirect Costs: Indirect costs are limited to a maximum of 25 percent of budget items, excluding sub-contracts and equipment on which no indirect costs are payable. Human Subjects: The Center requires that Institutional Review Board approval for any procedures involving human subjects must be submitted with the application. Laboratory Animals: The Center endorses the NIH policies on the care and use of laboratory animals, and requires that any proposed experiment involving the use of experimental animals be approved by the Institutional Animal Care and Use Committee at the investigator's institution. Documentation of approval by the local animal care committee will be required. Research Abstract: A concise, descriptive summary of the project must be submitted with the appli- cation. A form is provided for this purpose. Completeness to Applications: Provide all information requested. The signature and typed names of the institutional officer and princi- pal investigator must be on the application. Notification After Review of Application: Investigators will be notified, in writing, of the decision on their proposal. Mailing Instructions: Include eleven copies and an original of each and every part of the applica- tion, plus two additional copies of the Research Abstract form. NOTE: Each of the eleven copies must be placed in a binder with a label containing the title of the application and the name of the principal investigator. Mail the application to: Center for Indoor Air Research 1099 Winterson Road, Suite 280 Linthicum, Maryland 2 i 090 BATCo US DOJ v Philip Morris
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Appendix A CIAR Membership CHARTER MEMBERS Philip Morris U.S.A. R.J. Reynolds Tobacco Company Lorillard Corporation Svenska Tobaks AB Brown & Williamson Tobacco Corporation REGULAR MEMBERS Hoechst Celanese Mead Paper Japan Tobacco Inc. ASSOCIATE MEMBERS Ecusta, Division of PH Glatfelter DIMON International Mundet International Ltd. Quest Intemalional Flavors, USA Shorewood Packaging Somerville Packaging Corp. Standard Commercial Corp. United Technologies Carrier Corp. Universal Corporation C~ /3ATCo US DOJ v Philip Morris
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BLANK SHEET BATCo US DOJ v Philip Morris
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Appendix B CIAR Peer Reviewers Eric W. Adams United Technologies Research Center Gerald Akland U.S. EPA Janet Arey University of California, Riverside San jay Ar0ra Virginia Polytechnic Institute Sleven D. Aust Utah State University A. J. Baker The University of Tennessee Rebecca Bascom University of Maryland Bryan R. Becker University of Missouri-Kansas City Iris R. Bell University of Arizona Collette L Bement TRC Environmental Corporation M. A. Benjaminson Touro College Janet Benson Lovelace ITRI Irwin H. Billick Gas Research Institute Malcolm N. Blumenthal University of Minnesota William K. Boyes U.S. EPA Hoy Bohanon R. J. Reynolds Tobacco Co. Terry Brennan Camroden Associates Klaus Brunnemann American Health Foundation Harriet Burge Hma,ard School of Public Health Gary R. Burleson U.S. EPA Robert Burrell West Virginia University Medical Center Robert Bush University of Wisconsin Hospital Silvana Camboni Ohio State Universi~ Neal Castagnoli, Jr. Virginia Polytechnic Institute Jeffrey Cheek University of California-Davis Bean T. Chen ITRI Qingyan Chen M.I.T. Department of Architecture Leslie L. Christianson University of lllinois-Urhana-Champaign Theodore Colton Boston University School of Public ttealth Emanuela Corsini NIEHS O BATCo US DOJ v Philip Morris
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Greg Cosma Colorado State University Daniel L. Costa U.S. EPA Dr. Lucia G. Costa Universi~." of Washington Derek L Croome UniversiO, of Reading - UK William E. Crouse Chemical Industry Institute of Toxicology Jennifer B. Cunningham TRC Environmental Corporation Salil K. Das Meharry Medical College R. Del Delumyea Jacksonville University Amin Dharamsi OId Dom#don Universi~. , Virginia Mirjana Djordjevic American Health Foundation Douglas W. Dockery Harvard School of Public Health Charles Dorgan Dorgan Associates Richard L. Dory University of Pennsylvania Hospital Russell T. Doweli Lake Erie College of Osteopathic Medicine Deborah M. Drechsler-Parks UniversiD, of California, Santa Barbara Kevin Driscoll Proctor & Gamble Lawrence K. Duffy Universi~. of Alaska Fairbanks D. L. Dungworth University of California-Davis Bonnie Dunn U.S. FDA David A. Eastmond University of California. Riverside M. Samy El-Shall Virginia Commonwealth University Hugh L. Evans NYU Medical Center Henry M. Fales National Institutes of Health Jin Bao Fang National Institute of Standards atld" Technology Timothy Ford Harvard School of Public Health Mark W. Frampton UniversiO, of Rochester Medical Center Bettina M. Francis University of lllinois-Urbana-Champaign Donald Gardner Inhalation Toxicology John Gatley Brookhaven National Laboratot3' Jeffrey Gearhart ICF Kaiser Engineers Inc. Robert C. Gesteland University of Cincinnati Thomas V. Getchell University of Kemucky Nicholas J. Giardino Brooks AFB Roger Gie~ Northeastern University BATCo US DOJ v Philip Morris
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Avery. Nelson Gilbert Synesthetics, Inc. Stephen L. Gilbert University of Arizona Matthew lan Gilmour University of North Carolina Leon R. Glicksman Massachusetts Institute of Technology Joao F. P. Gomes University of Lisbon Henry Gong, Jr. Rancho Los Amigos Medical Center Terry Gordon NYU Medical Center Ronald E. Gots National Medical Advisory Service, Inc. S. Niranjan Goud University of Kentucky Charles W. Graham Texas A&M University Robert Greene Thomas Jefferson Medical College Wayne H. Griest Oak Ridge National Laboratory Sergey A. Grinshpt~n University of Cincinnati Albert E Gunnison NYU Medical Center Fariborz Haghighat Concordia Uni~,ersit)' David Hajjar Cornell University Medical Center Victor Flasselblad Center for Hea#h Policy Research Education Alan Hedge Cornell University David Hemenway University of Vermont Doug C. Hittle Colorado State University Stuart A. Hoenig University. of Arizona Dietrich Hoffmann American Health Foundation John R. Hoidal UniversiO' of Utah Medical Center G. Thomas Holbrook Virginia Polytechnic Institute W. Elliott Homer Tulane University Medical Center Ronald Howell UniversiO' of South Florida Ling-Ling Hung U.S. Public Health Service Hilary I. lnyang Geoenvironmental Design and Research Inc. Roger A. Jenkins Oak Ridge National Laboratory Jennifer Johnting American Health Foundation Ren Jun Anhui Anti.Epidemic Station, China Marry S. Kanarek University of Wisconsin.Madison Medical School John G. Keller Apex Environmental, Inc. Randal J. Keller Universir), of Arkansas for Medical Sciences I| 0 BATCo US DOJ v Philip Morris
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2o S. James Kilpatrick Virginia Commonwealth University Soren Kjaergaard University of Aarhus Steven R. Kleeberger Johns Hopkins University Michael T. Kleinman UniversiO' of California.lrvine Lorry A. Klinger Rexair, Inc. Earl Knutson U.S. Department of Energy Wendy H. Koch TRC Environmental Corporation Loren Koller Oregon State Universi~., Petros Koutrakis Harvard School of Public Health Michael R. Kuhlman Battelle John Lacey Rothamsted, UK Souheil Laham Ottawa, Canada Susan M. Larson University of Hlinois-Urbana-Champaign Jerold A. Last Universio, of California-Davis Christopher Si-Lung Lau U.S. EPA Michael D. Lebowitz University of Arizona College of Medicine Bruce Lehnert Los Alamos National LaboratmT Samuel B. Lehmr Tulane UniversiO' Medical Center David Leith UniversiO, of North Carolina Estelle Levetin University of Tulsa Robert Lewis U.S. EPA Roger Lewis St. Louis University Waiter Lewis Washington University Paul F. Linden UniversiO, of Cambridge - UK Bill Linn Rancho Los Amigos Medical Center Franklin Loew Tufts University Tyler S. Lorig Washington & Lee University Sudarshan K. Loyalka UniversiO' of Missouri-Columbia Joseph Lstiburek Building Science Corp. Robert Luebke U.S. EPA B. Madhusudhan UniversiO' of Mysore, India Jeannette McGIone Dalhousie UniversiO' James J. McGrath U. S. EPA Milton Meckler Meckler Engineers Group 0 BATCo US DOJ v Philip Morris
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John H. Mennear Campbell University Daniel Menzel University of California-lrvine Robert Mercer Duke University Medical Center John W. Mitchell University of Wisconsin-Madison Somenath Mitra New Jersey Institute of Technology Maria T. Morandi University of Texas Philip R. Morey Clayton Environmental Consultants. inc. Brooke Mossman University o[ Vermont Thomas E. Mull Technology Resource Consulting Engineers, lnc. Stanley A. Mumma The Pennsylvania State University Donald E. Myers University of Arizona Niren L. Nagda ENERGEN Consulting, Inc. William Nazaroff University of California-Berkeley Abroad Nevissi University of Washington P. J. Nieholls Welsh School of Pharmacy Gunnar Nielson Danish National Institute of Occupational Health Marc Nishimoto NOAA Michael W. O'Callaghan Tufts University Carol O'Neil Tulane University Medical Center Mary Kay O'Rourke University of Arizona College of Medicine Michael Ogden R. J. Reynolds Tobacco Co. James Otten Camber Corp. David Otto U.S. EPA Haluk Ozkaynak Har~,ard School of Public Health Kenneth C. Palmer Wayne State University S. S. Parmar University of North Dakota Darrell W. Pepper University of Nevada-Los Vegas Sere H. Phan University of Michigan Medical School Sarah Pixley University of Cincinnati Charles G. Ploppcr University of California.Davis William T. Porter University of Tulsa Neil R. Pumford University of Arkansas for Medical Sciences J. Michael Ramsey Oak Ridge National Laboratory Rose Ramsey Oak Ridge National Laboratory ]3ATCo US DOJ v Philip Morris
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John Reif Colorado State Universi~. Parker C. Reist University of North Carolina-Chapel Hill Gary L. Ritter TRC Environmental Corporation John Roboz Mount Sinai School of Medicine Brian A. Rock The University of Kansas John M. Rogers U.S. EPA Charles Rohde Johns Hopkins Universi~." Mark J. Rood Unh'ersiO' of Illinois at Urbana-Champaign Herbert Rosenkranz Universit)' of Pittsburgh Gary Rosenthal Somatogen Inc. James RotlOn Florida International University John C. Rutledge Universi~ of California-Davis P. Barry Ryan The Rollins School of Public Health of Emory University Lisa Ryan U.S. EPA Ragnar Rylander University of Gothenberg, Sweden Namir Saman Cons~dtant Behzad S. Samimi San Diego State University Harry J. Sauer, Jr. Universio, of Missouri-Rolla Marcia Sawnor Erdman AnthotLv Consulting Engineers Dennis Schuetzle Ford Motor Company Mary Jane Selgrade U.S. EPA James M. Seltzer Indoor Hygienic Technologies Corp. Mihir Sen UniversiO, of No~re Dame Richard B. Setlow Brookhaven National Laboratoo' Vinod Kumar Sharma b~dira Gandhi Institute Richard Shaughnessy University of Tulsa S. A. Sherif University of Florida C. Y. Shaw IRC, Canada Joseph H. Shinn Lawrence Livermore National Laboratoo" Charles L. Sidman UniversiO' of Cincinnati Wayne Silver Wake Forest University Jean D. Sipe Boston Universi~. School of Medicine Douglas A. Smith University of Toledo Raymond A. Smilh Universi~. ' of Nebraska Medical Center BATCo US DOJ v Philip Morris
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Jerome J. Solomon NYU Medical Center E. William Spannhake Johns Hopkins University Donald H. Stedman University of Denver Linda D. Stetzenbach University of Nevada-Las Vegas Thomas H. Stock University of Texas School of Public Health Jan Stolwijk Yale University School of Medicine Gary D. Stoner Ohio State University David C. Straus Texas Tech University Health Sciences Center Bruce Stuart ManTech Environmental Technologies Kerry Sublette University of Tulsa David L. Swift Johns Hopkins University You-Zhi Tang Bovar.Concord Environmental Robert W. Temple GulfCreat International, Inc. Nell W. Tindale Texas A&M Un&ersity Greg Traynor Lawrence Berkeley Laboratory. Simon Turner Healthy Buildings International Walter S. Tyler University of California-Davis James Ultman Penn State University Peter Valberg Gradient Corp. Gary Van Berkel Oak Ridge National Laboratory Karen M. Vetrano TRC Environmental Corporation James H. Vincent Unh,ersity of Minnesota Jamboor K. Vishwanatha University of Nebraska Medical Center Lance Wallace U.S. EPA John Weisburger American Health Foundation Kenneth J. Welch S. C. Johnson & Son, Inc. Janell D. Wenger Johnson Controls, Inc. Art Wheeler Wheeler Engineering Jeffrey Whitsert Children's Hospital Research Foundation Marshall Williams The Ohio State University Marsha Wills-Karp The Johns Hopkins University Tomasz Wihowski Southern Illinois University John Wispe Children's Hospital Medical Center Hanspeter Witschi University of California-Davis 0 0 BATCo US DOJ v Philip Morris
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James Yager Johns Hopkins University Medical Center Chin S. Yang P & K Microbiology Services Hsu-Chi Yeh Lovelace ITRI Vali Yousefi National Centre for Occupational Health South Afi'ica Paolo Zannetti Failure Analysis Associates, Inc. Judith T. Zelikoff NYU Medical Center Jianshun Zhang, Ph.D. National Research Council Canada Yuanhui Zhang Prairie Swine Centre Inc. BATCo US DOJ v Philip Morris
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Appendix C Guidelines for Final Report to ClAR The provision of the final report to CIAR is a major contractual responsi- bility of the CIAR-sponsored principal investigator. It is a comprehensive account to the funding organization of all work accomplished with monies supplied by the organization toward the objectives and specific aims set out in the approved version of the investi- gators' proposal. The f'mal report should contain: - A description of the original objec- tives and intentions, the rationale for the objectives, and reasons for research redirections. - A complete data report including tables and graphs, and descriptions of methodologies used to obtain the data. - Interpretive results. That is, how was the data evaluated and what do they mean? - Principal Investigator's summary and conclusions. -If applicable, brief suggestions for specific future research aims directly related to the stated objectives. - A comprehensive list of all abstracts, oral presentations, and joumal manuscripts (submitted, in press,and published) which resulted from CIAR-supported work. Please include reprints, preferably origi- nals, for any published works acknowledging CIAR support not already sent to CIAR. The final report is a technical docu- ment subject to peer review for scientific clarity and soundness and, therefore, should communicate the project objectives, design, and conclusions well. The f'mal report should not contain new proposals whether or not related to the work reported therein. Adherence to these guidelines will facilitate a timely f'mal report approval, disbursement of withheld dollars, and contract termination. BATCo US DOJ v Philip Morris
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The Center for Indoor Air Research wishes to acknowledge the assistance of the following: The Health Effects Institute (HEI) for sharing their Request for Application and mailing list. Portions of this RFA were based on the application proce- dures and administrative policies developed by HEI. Our use of their material recognizes the considerable efforts they have made to produce an effective application and administrative policy that meets the needs of both the contracting agency and the researchers. Use of this material does not imply, nor is there any association between our two organizations; The U.S. Department of Health and Human Services as portions of the application forms and instructions were modeled on the Grant Application Form PHS 398. BATCo US DOJ v Philip Morris
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Research Abstract Title of Project: Investigator(s): Institution: ABSTRACT: In the space below, please provide a descriptive summary of your proposed research project. Signature, Principal Investigator Date ~0 0 0 0 0 BATCo US DOJ v Philip Morris
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Application for Research Contract CENTER FOR INDOOR AIR RESEARCH 1099 Winterson Road, Suite 280, Linthicum, MD 21090 (410) 684-3777 FAX (410) 684-3729 1. Principal Investigator. Name, Title, Telephone ~, and mailing addre~. fa) (b) (c) Name T, de Telephone #/Fax * (d) (e) [~anmant Institution (0 Mailing Address Star efZip 2. Project Title. 3. Key Words. Please provide three (3) key words which will be used as reference headings. 4. Institution. Name and address of institution responsible and accountable for disgx~ition of funds awarded on the basis of this application. (a). (b) Institution Street Address (c). (d) Ciqt State~ip 5. Location. List location where research will be conducted if other than instituion identified in .4 above. 6. Inclusive Dates and Total Costs of this specific project related to each 12 month period if more than one year is required to com- plete project. Summarize from budget page, item 14(j). It must be understood that awards for 2nd and 3rd periods are dependent on Center approval of continuation application. Inclusive Date Total Cost (a) 1st 12 month period ~__ $ (b) 2nd 12 month period (if required) r.hnl_ $ (c) 3rd 12 month period (ifm=luired). .thru $ 7. Institutional Officer. Name, title and telephone number of individual authorized to s:gn for the institution identified in *4 above. It is understood that the officer, in applying for a contract, has read and found acceptable the Center's Management of Research Contracts and Contract Administration Policy. Name Telephone 8. Aims* (a) Hypoth~ (h} Objectiv~ 9. Significance of Proposed Work*. (a) ~ (h) (c) Importance of Project 10. Preliminary Studies*. (a) Fo~ibili~, of Propoxd I~--arch (b) Qualifications oflnv~agator 11. Experimental Plan*. (a) D~i~ (h) Merhod~ (c) Anal~i~ of data (d) interpretation ofr~ul~ (e) Timetable for the invesriOrion (f) Literature cited 12. Available Facilities and Resources*. 13. Other Support* Title (a) (e) Signature of Institutional Officer Date *Al~end as much material as ~luired. TYPE, single space, use 8-1/2" x 11" white paper and label each sheet with name of the principal investigator in the upper right hand comer and page number at the bottom. Consecut|vely number each addendum beginning with page 4. Do not insert pages between form pages FI and F3. Include eleven copie~ and an original. If sending photog~phs, include I original set. Note: Each of the eleven copies nma be bound per mailing instructions. O O BATCo US DOJ v Philip Morris
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14. Budget. Detail specific needs for the first 12-month period. Estimate cattegor3, sub-totals for 2nd and 3rd periods, if required. Append justifications. (a) Salaries, List personnel by name and ntle. Indicate individuals % time to be slxen~ on this project. Technical: Fringe Benefits payable at institution's rate of % Categoq, (a) SubTotal Ih) Comultants (per diem, travel & expeme~): Ic) Supplies & Expenses: Consumables (by categor’) Animals and related costs Othe’ Expenses (itemize) Category (b) SubTotal Catego~/(c) SubTotal (d) Travel Expenses: Category (d) SubTotal (e) Alterations and Renovations Categor’ (e) SubTotal Category (0 SubTotal Subcontracts (g) Equipment Catego~ (g) SubTotal (h) TOTAL DIRECT COSTS $ $ $ period 2nd period 3rd period (i) lndiaxt corn not to exceed 25% d the sum of (a) thin (e): (j) TOTAL PROJECTS COSTS 15. Biographical Sketch of all professional personnel listed in 14(a). Append. Please include the following: Name, title, education, scientific field, major research interest and/or professional experience and publications. (Limit list of publications to the 20 most important and/or relevant,) 16. a) Are Human Subjects to be used in this research? Yes If yes, attach Institutional Review Board approval for procedures involving human subjects. No b) Are Laboratory Animals to be used in this research? Yes No If yes, attach Institutional Animal Care and Use Committee approval for procedures involving animals. 17. Signature of Principal Investigator: Signature of Principal Investigator Date BATCo US DOJ v Philip Morris
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Board of Directors Charles R. Green, Ph.D., Chairman $co~t Appleton, Ph.D. Richard A. Carchman, Ph.D. J. Daniel Heck, Ph.D. Lutz Mueller, Ph.D. Helmut M. Reif, Ph.D, Tilford Rieh! Alex W. Spears, Ph.D. Inger Wahlberg, Ph.D. Executive Director Max Eisenberg, Ph.D. Staff Marsha S. Buss, C.P.A., Program Manager Administration Lynn Kosak-Channing, Ph.D., Staff Scientist Alice V. Zeiger, Ph.D., M.B.A., Staff Scientist Paula G. Raimondo, M.L.S., Manager of Library Sen,ices V. Christine MarquardL Administrative Assistant BATCo US DOJ v Philip Morris
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.I CENTER FOR INDOOR AIR RESEARCH 1099 Winterson Road, Suite 280 Linthicum, Maryland 21090 (410) 684-3777 FAX (410) 684-3729 E-mail: ciarinc@aol.com BATCo US DOJ v Philip Morris
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ATTACHMENT TO FOLLOWING DOCUMENT 0 0 0 BATCo US DOJ v Philip Morris
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