Things To Do Immediately About Master Validation Plan 2019

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Category Engineering, Production, Operations, Marketing, Software Validation

Deadline: January 27, 2019 | Date: January 29, 2019

Venue/Country: Online, U.S.A

Updated: 2018-11-07 15:12:39 (GMT+9)

Call For Papers - CFP

How to develop or improve upon a Master Verification and Validation Plan and System that meets U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements.

Why should you Attend:

The billions of dollars spent by industry annually for V&V are not providing the product safety or efficacy seemingly promised. For most companies, the fixes are not rocket-science, but proper up-front V&V planning and execution, documented in a corporate MVP and implemented by other V&V documents.

Areas Covered in the Session:

The 11 key documents for software validation

Incorporating 21 CFR Part 11 requirements

Suggested "test case" formats

Who Will Benefit:

Engineering

Production

Operations

Senior Management in Drugs

Speaker Profile:

John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses.

Event Fee: One Dial-in One Attendee Price: US $290.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: compliance4all14gmail.com