2-day In-person Seminar on Verification/Validation - Product, Process, Software and QMS at Las Vegas

Date:
01/16/2013 to 01/17/2013
Time:
5:00PM to 2:00AM
Price:
$1295
Venue:
Las Vegas, Las Vegas Nevada United States
Map:
Event Google Map
Contact:
Event Coordinator
Phone:
800-447-9407
Email:
Event Contact
Web:
Event Website

This course will review the company Master Validation Plan for major key inputs and CGMP deficiencies. It will address the FDA's newer and tougher regulatory stance. This course's aim is to prove "Product Risk Based V&V" by sufficient, targeted and documented risk-based V&V test case elements/scripts. It will teach participants to evaluate its elements against ISO 14971 and ICH Q9 for hazard analysis and product risk management.



This course will evaluate different field-tested, U.S. FDA-reviewed V&V protocols; how to employ equipment/process Requirements Specs / DQs, IQs, OQs, and PQs, or their equivalents per ASTM E2500, all against a background of limited company resources.



It will review a matrix that simplifies "as-product", in-product", process and equipment, et al, software VT&V, to assure key FDA requirements are not overlooked. While considering the QMS and 21 CFR Part 11; this course will make practical application of these same in two hands-on sessions.



DATE AND VENUE:

Location: Las Vegas | NV|January 17th & 18th, 2013

Conference Timings: 9 AM to 6 PM EST

WILL BE ANNOUNCED SOON

Price $1,295.00



Contact Information:

GlobalCompliancePanel

Event Coordinator

Toll free: 800-425-9409

Fax: 302-288-6884

http://www.globalcompliancepanel.com

Email: support@globalcompliancepanel.com

Price: $1,295.00

GlobalCompliancePanel,

USA, Livermore Common, Fremont,

CA 94539, USA Phone: 1800 425 9407

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