2014 - Webinar On Good Laboratory Practice Regulations

This web seminar presents an overview of FDA’s GLP regulation ? 21 CFR Part 58. The FDA GLP regulation complies with all GLP requirements globally. This web seminar covers every section of the FDA GLP regulation, offers FDA interpretation and provides an understanding of nonclinical safety research on a global basis. The web attendee with obtain a foundation of knowledge about FDA, the GLP regulation and nonclinical studies.
This webinar is a must for those personnel that require an understanding of the regulations governing laboratory activities relative to nonclinical testing that support or are intended to support applications for products regulated by FDA.
Areas Covered in the Session :
FDA's GLP regulations: 21 CFR Part 58
Objectives and concepts of GLP
Required GLP Studies
Responsibilities of different personnel
Data generation and evaluation
How to implement GLP’s
FDA interpretation of 21CFR Part 58
Who Will Benefit:
A must attend webinar for:
Regulatory Affairs Personnel
Quality Personnel
Clinical Personnel
Research Personnel
Laboratory Personnel
GLP auditors
GLP study directors
Manufacturing Personnel
Legal Personnel
Auditors
Training Departments
Clinical Research Associates
Consultants
Personnel who require a general understanding of the FDA’s GLP regulation ? 21 CFR Part 58
Price Tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
For more information contact
Compliance Trainings
5939 Candlebrook Ct,
Mississauga, ON L5V 2V5,
Canada
Customer Support : 416-915-4458
Email : support-AT-compliancetrainings.com