Improve Research Reproducibility A Bio-protocol resource
- Home
- Protocols
-
Concise Method
Standard protocol approvals, registrations, and patient consents
Request a Protocol
Ask a
question
Favorite
The study protocol was approved by the Independent Scientific Advisory Committee of the CPRD (protocol 17_219R2) and by the Research Ethics Committee of the Jewish General Hospital, Montreal, Québec, Canada. Written consent from participants was not required because of the use of anonymized data and no direct patient involvement.
Copyright and License information: ©2019 American Academy of Neurology
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.
Post a Question0 Q&A
