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Neurodevelopmental Disorders, Traumatic Brain Injury, Traumatic Spinal Cord Injury, Movement Disorders, Brain Tumors, Cerebrovascular Disorders, CNS Infectious Disorders, Epilepsy clinical studies support, clinical data management, pharmacovigilance, quality assurance, validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research, pain, stroke, diabetes, depression, insomnia, substance abuse, myasthenia gravis, Parkinson's disease, Alzheimer's disease, rheumatoid arthritis, multiple sclerosis, lupus, sepsis, head injury, osteoporosis, interstitial cystitis, vascular dementia, Desert Storm syndrome, Bethesda, Rockville, Maryland, national institutes of health, nih, biotechnology, biotech, Maryland, genes, bt, genetics, biomanufacturing, CROs, contract research organizations, service providers, contract research organization, CRO, contract research organisation, clinical research, pharmaceutical, biotechnology, contract research organizations, clinical research consultants, clinical trials consultants, clinical research, consultants, physicians, medical writers, technical writers, biotechnology, biotechnology companies, biotech companies, clinical studies, pharmaceuticals, pharmaceutical drugs,  medical investigators, medical researchers, 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system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research, dermatology,project management,patient registries,outreach programs,data management,biostatistics,global submissions,international,safety surveillance,medical writing, FDA, drug therapy,biomedical,virology,acquired immune deficiency,multiple sclerosis,migraine,headache,epilepsy,depression,smoking cessation,pregnancy,pregnant,psoriasis,dermatitis,prostate cancer,colorectal cancer, breast cancer,immune,thrombocytopenic,purpura,malignancies,hypertension,clinical drug trials,medical research, genetic research, drug testing, pharmacological agents, neuropsychiatric, disorders, depression,stroke, anxiety, psychosis, genetics, genomics, pharmacogenetics,Alzheimer's disease, Dementia Disorders, Neuropsychiatric Disorders, Affective Disorders, Neurodevelopmental Disorders, Traumatic Brain Injury, Traumatic Spinal Cord Injury, Movement Disorders, Brain Tumors, Cerebrovascular Disorders, CNS Infectious Disorders, Epilepsy validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research, pain, stroke, diabetes, depression, insomnia, substance abuse, myasthenia gravis, Parkinson's disease, Alzheimer's disease, rheumatoid arthritis, multiple sclerosis, lupus, sepsis, head injury, osteoporosis, interstitial cystitis, vascular dementia, Desert Storm syndrome, Bethesda, Rockville, Maryland, national institutes of health, nih, biotechnology, biotech, Maryland, genes, bt, genetics, biomanufacturing, CROs, contract research organizations, service providers, contract research organization, CRO, contract research organisation, clinical research, pharmaceutical, biotechnology, contract research organizations, clinical research consultants, clinical trials consultants, clinical research, consultants, physicians, medical writers, technical writers, biotechnology, biotechnology companies, biotech companies, clinical studies, pharmaceuticals, pharmaceutical drugs,  medical investigators, medical researchers, 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development,clinical research,international clinical trials,HIV,AIDs, virology,infectious diseases,global clinical trials, gastroenterology,respiratory, cardiovascular,oncology,dermatology,project management,patient registries,outreach programs,data management,biostatistics,global submissions,international,safety surveillance,medical writing, FDA, drug therapy,biomedical,virology al text here pharmaceutical companies, pharmaceutical development, pharmaceuticalproduct development, clinical research, biotech research, clinicaltrial, contract research organizations, contract research organisations, CRO, research development, discovery research, PPD, ppdi, Biotechnology,Biopharmaceutical,Pharmaceutical,medical device, clinical research,clinical trial,clinical study,clinical investigator,study site,medical affairs,regulatory affairs,clinical research organization,service management organization, market research,cancer market,oncology market,hematology market,due diligence, corporate partnering,medical advisory board,scientific advisory board, pharmaresearch, CRO,pharmaceutical development,clinical development,clinical research,international clinical trials,HIV,AIDs, virology,infectious diseases,global clinical trials, gastroenterology,respiratory, cardiovascular,oncology,dermatology,project management,patient registries,outreach programs,data management,biostatistics,global submissions,international,safety surveillance,medical writing, FDA, drug therapy,biomedical,virology,acquired immune deficiency,multiple sclerosis,migraine,headache,epilepsy,depression,smoking cessation,pregnancy,pregnant,psoriasis,dermatitis,prostate cancer,colorectal cancer, breast cancer,immune,thrombocytopenic,purpura,malignancies,hypertension,clinical drug trials,medical research, genetic research, drug testing, pharmacological agents, neuropsychiatric, disorders, depression,stroke, anxiety, psychosis, genetics, genomics, pharmacogenetics,Alzheimer's disease, Dementia Disorders, Neuropsychiatric Disorders, Affective Disorders, Neurodevelopmental Disorders, Traumatic Brain Injury, Traumatic Spinal Cord Injury clinical studies support, clinical data management, pharmacovigilance, quality assurance, validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research, clinical studies support, clinical data management, pharmacovigilance, quality assurance, validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research
clinical studies support, clinical data management, pharmacovigilance, quality assurance, validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research, pain, stroke, diabetes, depression, insomnia, substance abuse, myasthenia gravis, Parkinson's disease, Alzheimer's disease, rheumatoid arthritis, multiple sclerosis, lupus, sepsis, head injury, osteoporosis, interstitial cystitis, vascular dementia, Desert Storm syndrome, Bethesda, Rockville, Maryland, national institutes of health, nih, biotechnology, biotech, Maryland, genes, bt, genetics, biomanufacturing, CROs, contract research organizations, service providers, contract research organization, CRO, contract research organisation, clinical research, pharmaceutical, biotechnology, contract research organizations, clinical research consultants, clinical trials consultants, clinical research, consultants, physicians, medical writers, technical writers, biotechnology, biotechnology companies, biotech companies, clinical studies, pharmaceuticals, pharmaceutical drugs,  medical investigators, medical researchers, biologicals, fda, food and drug administration, regulatory affairs, submissions, pharmaceutical companies, product licenses, manuscripts, biopharmaceuticals, medical  writing, contract research organizations, CRO, drug discovery and drug development, pharmaceutical, biotechnology, discovery, preclinical, early clinical research, bioanalytical, clinical research, central lab, phase I, phase II, phase III, phase IV, formulation & manufacturing, clinical trials, investigators, study participation, ppd, drug development, pharmaceutical companies, pharmaceutical development, pharmaceuticalproduct development, clinical research, biotech research, clinicaltrial, contract research organizations, contract research organisations, CRO, research development, discovery research, PPD, ppdi, Biotechnology,Biopharmaceutical,Pharmaceutical,medical device, clinical research,clinical trial,clinical study,clinical investigator,study site,medical affairs,regulatory affairs,clinical research organization,service management organization, market research,cancer market,oncology market,hematology market,due diligence, corporate partnering,medical advisory board,scientific advisory board, pharmaresearch, CRO,pharmaceutical development,clinical development,clinical research,international clinical trials,HIV,AIDs, virology,infectious diseases,global clinical trials, gastroenterology,respiratory, cardiovascular,oncology,dermatology,project management,patient registries,outreach programs,data management,biostatistics,global submissions,international,safety surveillance,medical writing, FDA, drug therapy,biomedical,virology,acquired immune deficiency,multiple sclerosis,migraine,headache,epilepsy,depression,smoking cessation,pregnancy,pregnant,psoriasis,dermatitis,prostate cancer,colorectal cancer, breast cancer,immune,thrombocytopenic,purpura,malignancies,hypertension,clinical drug trials,medical research, genetic research, drug testing, pharmacological agents, neuropsychiatric, disorders, depression,stroke, anxiety, psychosis, genetics, genomics, pharmacogenetics,Alzheimer's disease, Dementia Disorders, Neuropsychiatric Disorders, Affective Disorders, Neurodevelopmental Disorders, Traumatic Brain Injury, Traumatic Spinal Cord Injury, Movement Disorders, Brain Tumors, Cerebrovascular Disorders, CNS Infectious Disorders, Epilepsy clinical studies support, clinical data management, pharmacovigilance, quality assurance, validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research, pain, stroke, diabetes, depression, insomnia, substance abuse, myasthenia gravis, Parkinson's disease, Alzheimer's disease, rheumatoid arthritis, multiple sclerosis, lupus, sepsis, head injury, osteoporosis, interstitial cystitis, vascular dementia, Desert Storm syndrome, Bethesda, Rockville, Maryland, national institutes of health, nih, biotechnology, biotech, Maryland, genes, bt, genetics, biomanufacturing, CROs, contract research organizations, service providers, contract research organization, CRO, contract research organisation, clinical research, pharmaceutical, biotechnology, contract research organizations, clinical research consultants, clinical trials consultants, clinical research, consultants, physicians, medical writers, technical writers, biotechnology, biotechnology companies, biotech companies, clinical studies, pharmaceuticals, pharmaceutical drugs,  medical investigators, medical researchers, biologicals, fda, food and drug administration, regulatory affairs, submissions, pharmaceutical companies, product licenses, manuscripts, biopharmaceuticals, medical  writing, contract research organizations, CRO, drug discovery and drug development, pharmaceutical, biotechnology, discovery, preclinical, early clinical research, bioanalytical, clinical research, central lab, phase I, phase II, phase III, phase IV, formulation & manufacturing, clinical trials, investigators, study participation, ppd, drug development, pharmaceutical companies, pharmaceutical development, pharmaceuticalproduct development, clinical research, biotech research, clinicaltrial, contract research organizations, contract research organisations, CRO, research development, discovery research, PPD, ppdi Biotechnology,Biopharmaceutical,Pharmaceutical,medical device, clinical research,clinical trial,clinical study,clinical investigator,study site,medical affairs,regulatory affairs,clinical research organization,service management organization, market research,cancer market,oncology market,hematology market,due diligence, corporate partnering,medical advisory board,scientific advisory board, pharmaresearch, CRO,pharmaceutical development,clinical development,clinical research,international clinical trials,HIV,AIDs, virology,infectious diseases,global clinical trials, gastroenterology,respiratory, cardiovascular,oncology, clinical studies support, clinical data management, pharmacovigilance, quality assurance, validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research, dermatology,project management,patient registries,outreach programs,data management,biostatistics,global submissions,international,safety surveillance,medical writing, FDA, drug therapy,biomedical,virology,acquired immune deficiency,multiple sclerosis,migraine,headache,epilepsy,depression,smoking cessation,pregnancy,pregnant,psoriasis,dermatitis,prostate cancer,colorectal cancer, breast cancer,immune,thrombocytopenic,purpura,malignancies,hypertension,clinical drug trials,medical research, genetic research, drug testing, pharmacological agents, neuropsychiatric, disorders, depression,stroke, anxiety, psychosis, genetics, genomics, pharmacogenetics,Alzheimer's disease, Dementia Disorders, Neuropsychiatric Disorders, Affective Disorders, Neurodevelopmental Disorders, Traumatic Brain Injury, Traumatic Spinal Cord Injury, Movement Disorders, Brain Tumors, Cerebrovascular Disorders, CNS Infectious Disorders, Epilepsy validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research, pain, stroke, diabetes, depression, insomnia, substance abuse, myasthenia gravis, Parkinson's disease, Alzheimer's disease, rheumatoid arthritis, multiple sclerosis, lupus, sepsis, head injury, osteoporosis, interstitial cystitis, vascular dementia, Desert Storm syndrome, Bethesda, Rockville, Maryland, national institutes of health, nih, biotechnology, biotech, Maryland, genes, bt, genetics, biomanufacturing, CROs, contract research organizations, service providers, contract research organization, CRO, contract research organisation, clinical research, pharmaceutical, biotechnology, contract research organizations, clinical research consultants, clinical trials consultants, clinical research, consultants, physicians, medical writers, technical writers, biotechnology, biotechnology companies, biotech companies, clinical studies, pharmaceuticals, pharmaceutical drugs,  medical investigators, medical researchers, biologicals, fda, food and drug administration, regulatory affairs, submissions, pharmaceutical companies, product licenses, manuscripts, biopharmaceuticals, medical  writing, contract research organizations, CRO, drug discovery and drug development, pharmaceutical, biotechnology, discovery, preclinical, early clinical research, bioanalytical, clinical research, central lab, phase I, phase II, phase III, phase IV, formulation & manufacturing, clinical trials, investigators, study participation, ppd, drug development, pharmaceutical companies, pharmaceutical development, pharmaceuticalproduct development, clinical research, biotech research, clinicaltrial, contract research organizations medical investigators, medical researchers, biologicals, fda, food and drug administration, regulatory affairs, submissions, pharmaceutical companies, product licenses, manuscripts, biopharmaceuticals, medical  writing, contract research organizations, CRO, drug discovery and drug development, pharmaceutical, biotechnology, discovery, preclinical, early clinical research, bioanalytical, clinical research, central lab, phase I, phase II, phase III, phase IV, formulation & manufacturing, clinical trials, investigators, study participation, ppd, drug development, pharmaceutical companies, pharmaceutical development, pharmaceuticalproduct development, clinical research, biotech research, clinicaltrial, contract research organizations, contract research organisations, CRO, research development, discovery research, PPD, ppdi, Biotechnology,Biopharmaceutical,Pharmaceutical,medical device, clinical research,clinical trial,clinical study,clinical investigator,study site,medical affairs,regulatory affairs,clinical research organization,service management organization, market research,cancer market,oncology market,hematology market,due diligence, corporate partnering,medical advisory board,scientific advisory board, pharmaresearch, CRO,pharmaceutical development,clinical development,clinical research,international clinical trials,HIV,AIDs, virology,infectious diseases,global clinical trials, gastroenterology,respiratory, cardiovascular,oncology,dermatology,project management,patient registries,outreach programs,data management,biostatistics,global submissions,international,safety surveillance,medical writing, FDA, drug therapy,biomedical,virology al text here pharmaceutical companies, pharmaceutical development, pharmaceuticalproduct development, clinical research, biotech research, clinicaltrial, contract research organizations, contract research organisations, CRO, research development, discovery research, PPD, ppdi, Biotechnology,Biopharmaceutical,Pharmaceutical,medical device, clinical research,clinical trial,clinical study,clinical investigator,study site,medical affairs,regulatory affairs,clinical research organization,service management organization, market research,cancer market,oncology market,hematology market,due diligence, corporate partnering,medical advisory board,scientific advisory board, pharmaresearch, CRO,pharmaceutical development,clinical development,clinical research,international clinical trials,HIV,AIDs, virology,infectious diseases,global clinical trials, gastroenterology,respiratory, cardiovascular,oncology,dermatology,project management,patient registries,outreach programs,data management,biostatistics,global submissions,international,safety surveillance,medical writing, FDA, drug therapy,biomedical,virology,acquired immune deficiency,multiple sclerosis,migraine,headache,epilepsy,depression,smoking cessation,pregnancy,pregnant,psoriasis,dermatitis,prostate cancer,colorectal cancer, breast cancer,immune,thrombocytopenic,purpura,malignancies,hypertension,clinical drug trials,medical research, genetic research, drug testing, pharmacological agents, neuropsychiatric, disorders, depression,stroke, anxiety, psychosis, genetics, genomics, pharmacogenetics,Alzheimer's disease, Dementia Disorders, Neuropsychiatric Disorders, Affective Disorders, Neurodevelopmental Disorders, Traumatic Brain Injury, Traumatic Spinal Cord Injury clinical studies support, clinical data management, pharmacovigilance, quality assurance, validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research, clinical studies support, clinical data management, pharmacovigilance, quality assurance, validation services, health research organizations, contract research organizations, cro, KAI, KAI-research, kunitz and associates, selma kunitz, rene kozloff, CDMS, washington dc, rockville, clinical trials, case report form, eCRF, Data Management, Coordinating Center, Remote Data Entry, Thin Client Computing, Citrix, NDA, Clinical data management,  Health research organizations, clinical studies support, protocol development, eCRF, electronic clinical data management system, clinical monitoring, statistical programming, clinical study report preparation, smart study, smart track, smart desk, smart CATI, computer assisted telephone interview, food and drug administration, FDA, quality assurance assessment, adverse event reporting, health policy, pharmaceutical clinical trials, outcomes research
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About KAI Research, Inc.
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     KAI's staff of over 50 full time employees includes senior project managers, physicians, Ph.D. researchers, clinical research associates (CRAs), information technology experts, database and web designers, statistical programmers, data managers, pharmacologists, and research assistants.

     Selma C. Kunitz, Ph.D. and Rene C. Kozloff, R.N., Ph.D., KAI's founders, integrate expertise in health and clinical studies, data management, and health care policy analysis to provide comprehensive corporate leadership.

STAFF PROFILES

Selma C. Kunitz, Ph.D. - President

      Dr. Kunitz, KAI's President, has repeatedly proven her ability to apply innovative methodology, technology, and organizational structures to clinical studies and is an expert in clinical data management and quality assurance. She is skilled in applying research methods to the design and conduct of collaborative clinical studies and in providing assurances of data integrity and quality. Dr. Kunitz serves as Principal Investigator for several NIH projects including the development of quality assurance guidelines, implementation of clinical trial quality assurance activities, and coordination and data management of multi-center clinical studies.

     She has lectured for pharmaceutical trade associations including the Drug Information Association (DIA) and Society for Clinical Data Management (SCDM) on quality assurance and data management. She serves on advisory and review committees for the NIH and other federal health agencies and serves as a consultant to academic institutions. In addition, she publishes and speaks on clinical research methods, clinical data base applications, quality assurance, and on issues in health care automation. She earned a Ph.D. in Behavioral Science/Social Epidemiology from the School of Hygiene and Public Health, Johns Hopkins University, M.S. in Management Information Systems/Organization Development from the American University and a B.A. In Economics from the University of Rochester.


Rene Kozloff, R.N., Ph.D. - Executive Vice President

     Dr. Kozloff, Executive Vice President and lead clinical researcher, is actively involved in clinical trials protocol development, subject recruitment and retention, clinical site staff training, study implementation, and report writing. Dr. Kozloff works with data management and statistical teams to assure the inclusion of clinical considerations in the design and implementation of study systems and analyses and writes clinical trials study reports for submission to the U.S. Food and Drug Administration (FDA).

     Dr. Kozloff heads KAI's efforts to define and validate multidisciplinary outcome measures for clinical trials and has introduced innovative techniques for gaining patients' perspectives on quality of life issues. She conducts focus groups of clinicians and potential subjects to develop outcome measures and focuses on minority health issues. She has developed subject recruitment and retention strategies for clinical studies.

     Dr. Kozloff was the Project Director for the DHHS Task Force on the Privacy of Private Sector Health Records.

     Dr. Kozloff has taught nursing and anthropology and has provided in-service training for clinicians, health professionals, and educators. She has lectured on a variety of subjects related to the social, psychological, economic, and familial influences on the need for and the use of health care, and is an accomplished writer. She served on review committees for the AHCPR (now AHRQ) and has published articles on a variety of health and policy issues. Dr. Kozloff earned a Ph.D. in Medical Anthropology from the Catholic University of America and a B.S. In Nursing from the University of Pennsylvania.



    Staff Profiles:

   • Selma Kunitz, Ph.D. 
   • Rene Kozloff, Ph.D.

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