FDA Regulations for Qualification and Validation Processes - 2017

In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient.

Why Should You Attend:

The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for analytical equipment qualification and validation in your facility?

Areas Covered in the Session:

• Requirements and approaches for Analytical Instrument Qualification
• Risk based validation approach
• Going through the qualification phases
• User requirements, writing the specifications

Who Will Benefit:

• Laboratory managers, supervisors and analysts
• IT managers and staff
• Consultants
• Laboratory suppliers of material, equipment and services
• Senior quality managers