Review a company's calibration, verification, and validation system against the critical requirements of the CGMPs and risk management. Starting with the required but often neglected Master Validation Plan, evaluating ISO 14971 and ICH Q9 risk analysis and documentation requirements in hazard analysis and product risk management, and a solid calibration program allows the development of meaningful product quality-specific equipment validations...

This webinar will detail a step-by-step procedure on how to write a practical, effective and compliant Standard Operating Procedures (SOPs), review and revise SOPs and maintain compliance over the course of the SOP lifetime. Why Should You Attend:Standard Operating Procedures (SOPs) are required for companies that are regulated. However, there is no guidance available by regulatory bodies on how to write, maintain, and update SOPs. Often, SOPs...