Compliance4All, Online Event
2017-04-28
Overview: 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
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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