Netzealous LLC DBA - Compliance4All, Online
2017-10-17
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: Risk based Validation Approach Going Through the Qualification Phases User Requirements, Writing the Specifications Testing and Deviation Handling Proper Documentation
Who Will Benefit: Quality Professionals Regulatory Professionals Compliance Professionals Production Supervisors Validation Engineers Manufacturing Engineers Production Engineers
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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