1st Regional Clinical Trials Workshop 2021
Organized by : ACRP
- To identify the applicable ICH guidelines in the conduct of clinical research trials.
- Will recognize the importance of human subject protection by way of informed consent and safety reporting.
- The participants will be provided with key tools to helpin their project and time management skills.
- Principle investigators
- Clinical research coordinators
- Data managers
- Research administrators
- IRB members
- Researcher of quality assurance
- Pharmaceutical companies
- Clinical research organizations
Kaimrc-RTE1@NGHA.MED.SA / +966 11 42 94369