Research With Drugs and Devices: Irbs, Industry and Investigators
Boston, MA: Public Responsibility in Medicine and Research [PRIM&R], 1990. 303 p.
Drugs; Industry; Investigators; Research; Drugs and Drug Industry; Human Experimentation Policy Guidelines / Institutional Review Boards; Informed Consent or Human Experimentation; Research on Special Populations; Third Party Consent; Economics of Health Care; Acquired Immunodeficiency Syndrome or HIV Infection;
Showing items related by title, author, creator and subject.
Unknown author (Public Responsibility in Medicine and Research [PRIM&R]; Tufts University. School of Medicine, 1990-11-01)
Financial Relationships in Clinical Research: Issues for Institutions, Clinical Investigators, and IRBs to Consider When Dealing With Issues of Financial Interests and Human Subject Protection: Draft Interim Guidance Unknown author (United States. Department of Health and Human Services.(DHHS) Office for Human Research Protections.(OHRP), 2001-01-10)
Guidance for Industry: Good Reprint Practices for the Distribution of Medical Journal Articles and Medical or Scientific Reference Publications on Unapproved New Uses of Approved Drugs and Approved or Cleared Medical Devices Unknown author (United States. Department of Health and Human Services. Food and Drug Administration [FDA]. Office of the Commissioner, Office of Policy, 2009-01)