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Key deadlines

Conference starts:

2017-08-04

Website

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Conference Description

Overview:
Many more typical questions are now available in this simple to understand, yet detailed training session designed to help manufacturers of FDA regulated products build a sustainable validation program.

Why you should attend:
How PLC-based systems or laboratory equipment should fall within the methods validation program, software validation program, or even the equipment qualification program.

Areas Covered In the Session:
Discuss what FDA is really looking for in process validation
Specify the deliverables associated with software validation
Common pitfalls to avoid when executing validation protocols
How to estimate costs and time associated with validation

Who will benefit:
Internal Auditors
Senior Management
Compliance Officers
QA Managers
QC Managers
Purchasing Managers

Speaker Profile:
Jonathan M. Lewis has over twenty-two years’ experience in the areas of executive management, quality control (QC), quality assurance (QA), manufacturing, regulatory affairs, validation, and project management in both industry and consulting roles. Mr. Lewis has experience in the medical device, diagnostic, biopharmaceutical, pharmaceutical, cosmetic, dietary supplement, food, and animal food industries.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com