Pharmaceuticals 2012 - US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus

This 6 hour virtual seminar will help you gain a comprehensive understanding of ICH GMPs and the nuances and differences between requirements in the US, EU and Japan. It will prepare you for regulatory inspections in these countries.

Why Should You Attend:

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).

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:

- Manufacturing

- Quality Assurance

- Senior management

- Project Managers

- Qualified Persons (QPs)

- Regulatory Compliance

- CMC Personnel

- Packaging Experts

- Auditors and Staff

- Consultants