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Things To Do Immediately About Master Validation Plan 2019

 
  November 27, 2018  
     
 
Netzealous LLC DBA - Compliance4All, Online
2019-01-29


Overview:
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

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

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com
 
 
Organized by: Event Manager
Invited Speakers:
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.
 
Deadline for Abstracts: 2019-01-28
 
Registration: https://www.compliance4all.com/control/w_product/~product_id=502268LIVE?channel=hum-molgen_Jan_2019_SEO
E-mail: compliance4all14@gmail.com
 
 
   
 
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