-
4th Nov 2016, 07:16 PM
#1
Requirements for Translation of Clinical Laboratory Documents
In a global clinical trial,
- Is it advisable to translate laboratory certifications or lab director qualifications to English? Both original language and translation would be stored in the Study TMF & Site files.
- Or is it acceptable for the Monitor to confirm in the monitor visit report that the documents were reviewed and found acceptable? In this case, translations would be provided on request from either auditor or health authority inspector.
Posting Permissions
- You may not post new threads
- You may not post replies
- You may not post attachments
- You may not edit your posts
-
Forum Rules