<--- Back to Details
First PageDocument Content
Science / Pharmacology / Medical statistics / Pharmaceutical industry / Medical ethics / Clinical trial / Human subject research / Informed consent / Food and Drug Administration / Research / Clinical research / Health
Date: 2013-07-19 18:52:25
Science
Pharmacology
Medical statistics
Pharmaceutical industry
Medical ethics
Clinical trial
Human subject research
Informed consent
Food and Drug Administration
Research
Clinical research
Health

Microsoft PowerPoint - Preparing_New_Study_1ppt [Compatibility Mode]

Add to Reading List

Source URL: www.research.ucsf.edu

Download Document from Source Website

File Size: 93,22 KB

Share Document on Facebook

Similar Documents

Client Disclosure and Informed Consent

DocID: 1vnrO - View Document

INFORMED CONSENT/PERMISSION FORM FOR EDUCATION TRIPS (Students Under 18 Years ) The Nipissing-Parry Sound Catholic District School Board is arranging a Summer School Physical Education Ice Hockey program Juy 2nd – July

DocID: 1vn2S - View Document

Gewebebank Bern Tel. Voranmeldung auf 23228  Informed Consent vorhanden  Chirurg....................................... Sucher........................................ Zeit (clamping)..........................

DocID: 1vj1g - View Document

INFORMED CONSENT ASSESSMENT FORM URERB Protocol Code: (to be filled out by URERB Secretariat)

DocID: 1vj0w - View Document

Informed Consent Form Checklist (Including Phase 1 Study) This checklist is designed to assist researchers in drafting, and CREC members in reviewing Informed Consent Forms (including Phase 1 Study). The checklist conta

DocID: 1v8vO - View Document