ResearchBib Share Your Research, Maximize Your Social Impacts
Sign for Notice Everyday Sign up >> Login

Main Menu

Searching By

PARTNERS

Contact us

FDA Validation 2012 - FDA Software Validation Self-Check ? plan an effective Internal Audit program

Date2012-05-09

Deadline2012-05-09

VenuePalo Alto, USA - United States USA - United States

KeywordsFDA software validation regulations; FDA software validation audits; passing FDA inspection; software quality processes; 21 CFR part 11 planning; FDA inspection process

Websitehttp://www.complianceonline.com/ecommerc...

Topics/Call fo Papers

This FDA software validation Webinar/training will discuss how to self audit and ensure validation and software quality processes that will pass FDA inspection.


Why Should You Attend:

FDA Commissioner Margaret Hamburg recently announced several new enforcement initiatives.They are certain to impact your regulatory risk profile. How will you prepare for software quality, software validation and 21 CFR part 11 planning?

Other CFPs

  1. Pharmaceutical Water System Use & Monitoring
  2. Equipment Calibration in FDA QSR ? Regulations and Warning Letters
  3. Acceptance Activities in FDA QSR ? Regulations and Warning Letters
  4. Making Risk-Benefit Decisions ? Preparing for the New FDA Guidance Documents
  5. Medical Device Risk Management Using ISO 14971

Last modified: 2012-03-06 18:46:39