<--- Back to Details
First PageDocument Content
Clinical research / Nursing research / Design of experiments / Pharmacology / Medical ethics / National Institutes of Health / Clinical trial / Institutional review board / Informed consent / Medicine / Health / Research
Date: 2014-08-27 16:04:18
Clinical research
Nursing research
Design of experiments
Pharmacology
Medical ethics
National Institutes of Health
Clinical trial
Institutional review board
Informed consent
Medicine
Health
Research

Points to Consider in Drafting

Add to Reading List

Source URL: gds.nih.gov

Download Document from Source Website

File Size: 46,55 KB

Share Document on Facebook

Similar Documents

Cell Biology and Cancer under a contract from the National Institutes of Health in collaboration with the National Cancer Institute

DocID: 1vqc4 - View Document

SCIENCE & TECHNOLOGY POLICY IN STITUTE Technology Development at the National Institutes of Health (NIH): Summary Report Brian L. Zuckerman

DocID: 1v9kv - View Document

DEPARTMENT OF HEALTH AND HUMAN SERVICES NATIONAL INSTITUTES OF HEALTH National Heart, Lung, and Blood Institute (NHLBI)

DocID: 1v3b2 - View Document

Conference Organizers James Prestegard, CFG and University of Georgia Michael Tiemeyer, CFG and University of Georgia John Hanover, CFG and National Institutes of Health Joyce Taylor-Papadimitriou, CFG and King’s Colle

DocID: 1v07l - View Document

Nematode sperm motility* Harold E. Smith§ National Institute for Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda MD, USA Table of Contents

DocID: 1uVU8 - View Document