Preparing for an FDA API GMP Inspection 2014 is a webinar that covers topics such as:
- What are the causes of GMP violations and why do they exist
- What are the most important short term actions?
- Identifying critical reviews to perform
- What are long term activities that help prepare the organization to succeed?
Preparing for an FDA API GMP Inspection 2014 is intended for:
- Supervisory personnel responsible for any API functions
- API and Excipient producers and consumers (Drug Product Firms)
- Materials Management - purchasing, warehousing and distribution
- Quality Management
- Laboratory Supervision
- R&D personnel associated with API methods, validations, cleaning procedures, scale ups and specifications
- Functions that have an interest in becoming familiar with API GMP and its business impact
- Manufacturing chemists, Engineers
