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Computer System Validation - Reduce Costs and Avoid 483s

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Website http://bit.ly/1yaEiaC | Edit Freely

Category 21 CFR Part 11 Compliance;

Deadline: June 15, 2017 | Date: June 15, 2017-June 16, 2017

Venue/Country: San Diego, U.S.A

Updated: 2017-05-10 21:12:08 (GMT+9)

Call For Papers - CFP

This Computer System Validation Training course will explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Today, the FDA performs both GxP and Part 11 inspections, the Europeans have released an updated Annex 11 regulation that expands Part 11 requirements and companies must update their systems and processes to maintain compliance.

Many companies outsource IT resources and are involved in Software as a Service (SaaS) and cloud computing. These vendors are not regulated, and therefore, regulated companies must ensure compliance for both infrastructure qualification and computer system validation to avoid FDA form 483s and Warning Letters.

Note: Use coupon code NB5SQH8N and get 10% off on registration.


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.