Laboratory Compliance 2012 - Archiving GLP Records: How Archiving Makes or Breaks the Audit
Date2012-03-22
Deadline2012-03-22
VenuePalo Alto, USA - United States
KeywordsGLP Records; Archiving Practices; Laboratory Records; on-site review; archive structure; archive facility; in-house archiving; out-sourced archiving; citations; archiving process
Topics/Call fo Papers
This webinar on archiving GLP records will discuss the options for managing large archiving facilities to small facilities with one-room archives. You will receive practical tips on how to correct mistakes that agencies have cited regarding archiving.
Why Should You Attend:
Regulatory agencies, FDA or EPA, depend on documents and samples to evaluate the proper conduct of GLP studies in retrospect. Sponsors have a critical responsibility to retain records and samples completely, well-organized, secure, accessible for agency review, and protected from physical damage.
Other CFPs
- Effective & Legal Documentation : If It Wasn’t Documented, It Didn’t Happen
- Foreign Manufacturing Facilities ? Avoiding Problems with FDA
- Foreign Manufacturing Facilities ? Avoiding Problems with FDA
- Issue Detection and Escalation in Clinical Trial Settings
- CFP - Advances in Multimedia - An International Journal (AMIJ)
Last modified: 2012-02-24 15:01:31