[
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
The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment)
Description
(External link) Statutory Instruments 2008 No. 941
Website address
The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008
