Equipment and Facility Qualification 2017
Equipment Qualification, process validation and commissioning have some overlapping areas.
Sun, Dec 10, 2017 10:00 AM (PST)
Online,
Fremont,
California
Questions? Contact Event Organizer
This event ended
Sun, Dec 10 - 11:00 AM
{{calendarLabel}}
{{dow}}
{{calDate.dayOfMonth}}
Sold Out
Ended
{{calDate.available}}
Visit Fundraiser Page
{{ campaign.name }}
Visit fundraiser page to {{ campaign.ctaLabel.toLowerCase() }}
Visit Fundraiser Page
{{ item.name }}
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: support@compliance4All.com
Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501615LIVE?channel=ticketprinting_Dec_2017_SEO
Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501615LIVE?channel=ticketprinting_Dec_2017_SEO
Cart is empty
Tickets
Price
Qty