Validation Program to a Building from Top to Bottom - 2017

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: [email protected]

Others Details

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