Best Practices & Effective Cleaning Validation Procedures - 2017

MessageThis Webinar is over
Date Sep 14, 2017
Time 10:00 AM
Cost 150.00
Online
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 Cleaning Validations of your

manufacturing equipment?

Areas Covered in the Session:
    Understand the FDA perspectives on cleaning validation and areas of

concern during regulatory inspections
    Be able to set up cleaning validation procedures, protocols and reports

that meet current FDA, WHO, PIC/S and EU regulations
    Prepare and defend your own cleaning validation approach/program and

avoid costly delays and/or rejections by regulatory agencies

Who Will Benefit:
Senior Quality Managers
Quality Professionals
Production Supervisors
Validation Engineers
Process Owners
Quality Engineers
Quality Auditors

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

 


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