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Analytical Instrument Qualification and Validation Processes - 2017

 
  August 09, 2017  
     
 
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
 
 
Organized by: Event Manager
Invited Speakers:
Speaker Profile:
Joy McElroy Upon earning a degree in Zoology at North Carolina State 

University, Joy made her debut in the pharmaceutical industry in 1992 at 

Pharmacia & UpJohn performing Environmental Monitoring and Sterility 

Testing. Her hard work allowed her to move into a supervisory role at Abbott 

Laboratories where she oversaw their uality Control Lab.
 
Deadline for Abstracts: 2017-10-16
 
Registration:
Full Details & Registration Link:
 
E-mail: support@compliance4All.com
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