APR 28

FDA Regulations for Qualification and Validation Processes - 2017

   

Conference CFP

  

 

When:

  28 Apr 2017 through 28 Apr 2017

CFP Deadline:

  28 Apr 2017

Where:

  Online Event

Website URL:

  http://www.compliance4all.com/control/w_product/~product_id=501119LIVE?channel=mailer&camp=Webinar&AdGroup=brownwalker_Apr_2017_SEO

Sponsoring organization:

  Compliance4All

Categories:

  Medicine & Health > Pharmaceutical/Medicinal

Event description:

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

Posting date:

01 March 2017
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Placement:

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