ComplianceOnline

White Paper: GLP Final Reports and Archival Practices – 7 Best Practices for Regulatory Compliance

  • By: ComplianceOnline
  • Date: July 08, 2014
Webinar All Access Pass Subscription Abstract:

Compliance with the principles of GLP (Good Laboratory Practices) is a legal requirement for test facilities. After each GLP study is completed or terminated, a GLP final report must be prepared for submission to the regulatory agency. Test facilities should follow GLP guidelines and good archival practices as non-compliance compromises the quality and integrity of the study and gives scope for rejections,warning letters and citations by the FDA. This white paper primarily intends to provide information about necessary documentation, requirements for GLP final reports, and also details about best practices to be followed in final reporting and archiving for regulatory compliance.

Bookmark and Share

Trending Compliance Trainings

Trial Master File and Clinical Data Management Regulated by FDA
By - Carolyn Troiano
On Demand Access Anytime
Good Documentation Practice and Record Keeping Regulations (FDA & EMA)
By - Dr. Afsaneh Motamed Khorasani
On Demand Access Anytime
GAMP Data Integrity 21 CFR Part 11 Training Course
By - Kelly Thomas
On Demand Access Anytime
NEW Reclamation Process - Fed Gov't Payments
By - Donna K Olheiser
On Demand Access Anytime
Understanding and Preparing for FDA Pharmaceutical Inspections
By - Michael Ferrante
On Demand Access Anytime
How to conduct an effective BSA Audit
By - Justin Muscolino
On Demand Access Anytime
Installation and Qualification of the Packaging Lines
By - John E Lincoln
On Demand Access Anytime
Best Sellers
You Recently Viewed
    Loading