US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection F (Pharmaceuticals Trai)
Venue: Online Event
|Event Date/Time: Jul 26, 2011||End Date/Time: Jul 26, 2011|
This full-day ICH GMP training course will provide your company the opportunity for a comprehensive understanding of ICH GMP and the nuances and differences between the three main ICH triumvirate regions (U.S. EU and Japan).
It will cover the key areas of how ICH was established, it's goals and objectives, expectations of the healthcare authorities involved and practical differences that you will experience in a GMP inspection of a facility by FDA, an EU Competent Authority or PMDA.
Who Will Benefit:
This Webinar will provide invaluable assistance to all License Owner personnel in the Pharmaceutical, Biotechnology and Combination Products areas, including contract manufacturers, packagers and suppliers. Particular functional expertise receiving value from attending would be:
- Quality Assurance
- Senior management
- Project Managers
- Qualified Persons (QPs)
- Regulatory Compliance
- CMC Personnel
- Packaging Experts
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