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).