EVENT
Contract Research Organization Guideline
e-Participation Events
About the Project
A regulatory guide for contractual research centers in the Kingdom of Saudi Arabia. The guide contains post-licensing regulations as follows:
1. Clinical Trials Request (CTAp) Process
2. Organizational work of Contract Research Centers (CRO) and the services provided.
3. Clinical Research Associate (CRA) employees.
4. Contracts and Agreements.
14/02/2022 - 14/03/2022
webmaster@sfda.gov.sa
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Last Modified Date: 17/02/2022 - 8:00 AM Saudi Arabia Time