Course Overview
This program is designed to provide professionals in the pharmaceutical industry with a comprehensive understanding of ethical principles and regulatory guidelines governing clinical trials. Participants will gain insights into various types of trials, documentation requirements, and the importance of hazard assessment and risk control measures.
Features
- Comprehensive understanding of ethical principles and regulatory guidelines governing clinical trials.
- Insights into different types of trials, documentation requirements, and risk management strategies.
- Awareness of emerging trends and innovations in regulatory affairs and their implications for trial management.
Target audiences
- Professionals in the pharmaceutical industry involved in clinical trial management, regulatory affairs, quality assurance, and drug development.
Instructor
