Meeting EMA’s Revised Guidelines on Computerized Systems and Electronic Records in Clinical Trials
Gain valuable insights and practical recommendations for meeting the European Medicine Agency’s (EMA) revised guidelines on computerized systems and electronic records in clinical trials.
Discover best practices for meeting the expectations of EMA’s revised guidelines:
- Ensure data integrity in clinical trials.
- Conduct thorough risk assessments.
- Implement electronic signatures effectively.
- Comply with new archiving requirements.
- Safeguard personal data with GDPR guidelines.
- Follow the validation process for computerized systems.
Download our white paper to learn how you can ensure compliance, data integrity, and the highest standards of quality in your clinical trial processes.
