Biopharmaceutical Manufacturing Process Validation Training Course
Module 1 is Free to Attend – Register Below
Learn more about the course (dates, price, skills gained, and when module 1 is) by visiting the course page.
Module 1 Overview | Overview of regulatory guidances
Live and Recorded | 60 Minutes
Overview of regulatory guidances
- Examine the relevant ICH guidances: Q8, Q9, Q10, Q11, Q12 Draft
- Understanding the EMA and FDA guidances on process validation
- Understand the reasoning for the requirements
- Comparison of traditional and enhanced development
Register for the free Module 1 by completing the form below. You will be sent joining instructions and more information about the course (agenda, trainers, pricing etc). If the live session has recently been delivered, you will be sent the latest recording.