Hybrid Quality Systems For Pharmaceuticals - Combining ICH Q7A & Part 210-211 is a webinar that covers topics such as:
- Jurans`s Quality Loop And Its Application T o Our Industry
- Quality 101
- Comparison of Part 210/211 & ICH-Q7A
- The Scope of the GMP`s
- Constructive Criticism of Part 210/211 & ICH-Q7A
- Praises and Accomplishments of Part 210/211 & ICH-Q7A
- A Quick Comparison to ICH & ISO
- The FDA Quality Systems Approach to the Pharmaceutical GMPs
- Planning and Implementing the Hybrid System
Hybrid Quality Systems For Pharmaceuticals - Combining ICH Q7A & Part 210-211 brings together:
- Interdepartmental functions associated with scaling up and commercializing a new medical product
- Quality control, Quality, engineering, regulatory, IT and manufacturing staff working in the FDA regulated industry in the development and manufacture of medical products
- Suppliers and software vendors, servicing the FDA regulated industries, who want to better understand the customer’s needs and requirements
- Regulatory Affairs working on approval of combination products
