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Conference

Good Documentation Practice for GxP Environments - Webinar By GlobalCompliancePanel

About this event

Web site
bit.ly/v7WUn4…
When
8 Dec 2011
Where
Online Training, Wilmington | DE | Zip 19801, United States
Organiser
GlobalCompliancePanel
Contact address
webinars web
online training webinar
Suite 1200
Wilmington
Delaware
United States
Tel
8004479407
Fax
3022886884
E-mail
webinars@globalcompliance…

This webinar will cover Good Documentation Practice for GxP environments. This webinar will explore what companies need to know to comply with regulations regarding documentation, what Good Documentation Practice is, what needs to be documented, why it is documented, and FDA expectations for documentation.

The webinar explores what the GxP regulations and guidance's say about Good Documentation Practice. Examples of both good and poor documentation are given and exercises demonstrate both good and poor practices.

Why you should attend: In today's strict regulatory environment it is more important than ever for companies and individuals to understand and practice good documentation to comply with FDA regulatory requirements. This webinar will cover Good Documentation Practice for GxP environments. Understand what needs to be documented, what FDA looks for in documentation, relevant regulations for documentation, and related guidance's.

Areas Covered In the Session:
FDA 101: who is the FDA, regulations, guidance's, documentation and me
Why document?
What needs to be documented?
What documentation does FDA look for during an inspection?
What do the GMP, GCP, and GLP regulations and guidance’s say about documentation?
Examples and exercises for good documentation
Summary/ Q&A
Who will benefit:
GxP personnel involved with GxP Documentation
R&D
Production
Quality
Regulatory

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884