Equipment and Facility Qualification 2017

Overview:
This webinar removes that confusion between equipment Qualification,

process validation and Facility commissioning.

Why should you Attend:
The Webinar is designed for Quality and Manufacturing in the

Pharmaceutical and Biopharmaceutical industries.

Areas Covered in the Session:
Quality Risk Management Defined
Compliance Requirements for Quality Risk Management
The Quality Risk Management Model
Quality Risk Management Life Cycle

Who Will Benefit:
Quality Engineers
Manufacturing Engineers
Line Managers

Speaker Profile:
Mr. Muchemu , MSc, MBA is the Co-founder and CEO of CGMP University

Inc. Training and consulting organization in San Jose, California. Mister

Muchemu is an established author of several GMP books. His background is

Chemical Engineering. He has worked in the Pharmaceutical, Medical Device

and Tissue industries for over fifteen years.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

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WHEN AND WHERE

11 December 2017
United States of America

ORGANIZER

Netzealous LLC DBA - Compliance4All

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Added 6 years ago by Compliance4All on Education