This seminar will be of particular inveterst to all those from the Pharmaceutical Industry working in: Development Manufacturing Engineering Quality Personnel from the Pharmaceutical and Biopharmaceutical Industry with the following background: Process Engineers Pharmacists Scientists Quality Assurance Professionals Quality Control Managers Late Stage Product and Process Development Engineers, Scientists, Pharmacists Technology Scale Up and Transfer Managers Validation and Qualification Managers Validation and Qualification Specialists Risk Management Specialists Lean Management Specialists Operations Managers, Engineers
The two day Process Validation in the US and EU, balancing Science and Risk during the Product Lifecycle meeting will help you gain an understanding of the EU and FDA Process Validation Guidance, learn how to establish a Process Validation Programme, under the link between Quality by Design and Process Validation as well as how to apply relevant tools for Process Validation including Risk Assessment.
WHY YOU SHOULD ATTEND
Benefits in Attending:
GBP EUR USD Standard 1299 1819 2026 Excluding VAT @ 20.00%