FDA Regulations for Qualification and Validation Processes - 2017

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: 

Requirements and approaches for Analytical Instrument Qualification

Risk based validation approach

Going through the qualification phases

User requirements, writing the specifications

Who Will Benefit:

Laboratory managers, supervisors and analysts

IT managers and staff

Consultants

Laboratory suppliers of material, equipment and services

Senior quality managers

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 Quality Control Lab.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com

Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501119LIVE?channel=mailer&camp=Webinar&AdGroup=ticketprinting_Apr_2017_SEO