Conference & Events
Event Details
21 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits - Webinar By GlobalCompliancePanel
This webinar details both regulations and provides details for implementing computerized systems.
Date: 01 May 2012 10:00 - 11:30
Event Subject(s):
Biosciences
Education
General
Venue
Online Training
1000 N West Street
Delaware
Suite 1200
Wilmington
19801
United States of America
Find this location using Google Map
Useful link:
Organiser Information
Organiser(s): GlobalCompliancePanel
Contact for Event Information
Name : Online Training
Address:
Online Training
1000 N West Street
Suite 1200
Wilmington
19801
United States of America
Tel:
800-447-9407
Fax:
302-288-6884
Email:
webinars@globalcompliancepanel.com
Contact Useful link:
http://www.globalcompliancepanel.com
Additional Information
Speaker Information:
David Nettleton, is an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation. His latest book is "Risk Based Software Validation - Ten easy Steps" that relates to the development, purchase, installation, operation and maintenance of computerized systems used in regulated applications. He specializes in performing gap analysis, remediation plans, SOP development, vendor audits, training, and project management. He has completed more than 185 mission critical software validation projects.
Useful link:
Other information:
Learn exactly what is needed to be compliant for all three primary compliance areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach. This webinar demystifies Part 11 and the new European equivalent Annex 11. It gets you on the right track for using electronic records and signatures to greatly increase productivity.
Areas Covered in the Session:
Which data and systems are subject to the regulations?
What the regulations mean, not just what they say.
Avoid 483 and Warning Letters.
Examine the regulatory requirements for the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation.
Ensure data integrity, security, and protect intellectual property.
Understand the current computer system industry standards for security, data transfer, and audit trails.
Electronic signatures, digital pens, and biometric signatures.
Evaluate the regulatory requirements related to the current computer system standards for security, data transfer, audit trails, electronic signatures, digital pens, and biometric signatures.
SOPs required for the IT infrastructure.
Product features to look for when purchasing COTS software.
Reduce validation resources by using easy to understand fill-in-the-blank validation documents.
Who Will Benefit:
IT
QA
QC
Laboratory staff
Managers
GMP, GCP, GLP professionals
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
