Enhance your skills in validating computerized systems with this specialized training course.
Hello friends,
Registration is now open for the most comprehensive course on Computerized Systems Validation Lifecycle, by HCE Med, which I will be leading.
The course covers regulatory requirements including:
- 21 CFR Part 11
- EU GMP-Annex 11
- GAMP 5 2nd edition guidance
- General Principles of Software Validation
- IEC 62304
- GAMP RDI
- MHRA
This hybrid comprehensive course spans 3 days, held once a week, and includes rich content addressing the entire software and computerized systems lifecycle. It is accompanied by practical examples from my extensive experience in the pharmaceutical and medical device industries.
For more details about this course and additional courses, and to register, please contact us soon as the number of spots is limited.
Email: heliyahu21@gmail.com
Phone: 050-577-4804