[
Skip to content
]
Site map
Accessibility
Text size:
Smaller
|
Normal
|
Larger
text only
National Research Ethics Service
Search our Site
Keywords
About NRES
News and publications
Training
Applications
Patients and the public
HRA Extranet
Useful links
Contact us
Home
»
Applications
»
Guidance
«
Applications
Approval requirements
Integrated Research Application System (IRAS)
Site-Specific Assessment
Booking and Submitting your application
After submission
Attending a REC meeting
After ethical review
Resubmission and Appeals
Providing feedback
Guidance
Clinical trials
Consent guidance and forms
Governance and directives
Guidance and good practice
Research guidance
Phase 1 trials guidance
Frequently asked questions
Glossary
Proportionate Review
HRA Ethics Officer Pilot
.
Title
Informed consent in CTIMPs
Description
NRES information paper on informed consent in clinical trials of investigational medicinal products
Issued date
May 2008
Document
Informed consent in CTIMPs.pdf
-
71KB
Informed consent in CTIMPs.pdf