Investigational Device Exemptions Manual

Investigational Device Exemptions Manual
Author :
Publisher :
Total Pages : 220
Release :
ISBN-10 : IND:30000105703528
ISBN-13 :
Rating : 4/5 (28 Downloads)

Synopsis Investigational Device Exemptions Manual by : Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance

Investigational Device Exemptions Manual

Investigational Device Exemptions Manual
Author :
Publisher :
Total Pages : 220
Release :
ISBN-10 : UOM:39015038600071
ISBN-13 :
Rating : 4/5 (71 Downloads)

Synopsis Investigational Device Exemptions Manual by : Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance

Staff Manual Guide Transmittal No. ...

Staff Manual Guide Transmittal No. ...
Author :
Publisher :
Total Pages : 24
Release :
ISBN-10 : MINN:31951D03729034G
ISBN-13 :
Rating : 4/5 (4G Downloads)

Synopsis Staff Manual Guide Transmittal No. ... by : United States. Food and Drug Administration

FDA Compliance Program Guidance Manual

FDA Compliance Program Guidance Manual
Author :
Publisher :
Total Pages : 34
Release :
ISBN-10 : MINN:31951D03732719D
ISBN-13 :
Rating : 4/5 (9D Downloads)

Synopsis FDA Compliance Program Guidance Manual by : United States. Food and Drug Administration

Premarket Approval (PMA) Manual

Premarket Approval (PMA) Manual
Author :
Publisher :
Total Pages : 144
Release :
ISBN-10 : SRLF:EE0000206813
ISBN-13 :
Rating : 4/5 (13 Downloads)

Synopsis Premarket Approval (PMA) Manual by : Center for Devices and Radiological Health (U.S.). Office of Device Evaluation

Protecting Study Volunteers in Research

Protecting Study Volunteers in Research
Author :
Publisher :
Total Pages : 392
Release :
ISBN-10 : UOM:39015061377969
ISBN-13 :
Rating : 4/5 (69 Downloads)

Synopsis Protecting Study Volunteers in Research by : Cynthia McGuire Dunn

Protecting Study Volunteers in Research is a suggested educational resource by NIH and FDA (source: NIH Notice OD-00-039, 2000, page 37841, Federal Registry 2002) and has become required reading in many academic institutions, IRBs, investigative sites, and for many Biopharmaceutical and CRO companies. This well-organized and concise manual teaches organizations how to successfully implement the highest standards of safe and ethical treatment of study volunteers while addressing current and emerging issues that are critical to our system of human subject protection oversight. Topics covered include: Conflicts of interest in research, Participant recruitment and retention in clinical trials, Research with secondary subjects, tissue studies, and records review, Historical perspectives on human subject research, Updated ethics and federal regulations, Roles and responsibilities of institutions and independent sites, Roles and responsibilities of investigators and the study process. --Amazon.com