This Event has Passed
Thursday, September 20, 2018
10:00 AM - 11:15 AM
10:00 AM - 11:15 AM See all dates and Times
http://www.compliance4all.com/control/w_product/~product_id=502097LIVE?channel=upcomingevents_Sep_2018_SEO
Overview: The webinar will have the answers. In addition, using industry proven case studies on how to avoid 483 inspectional observations and warning letters attendees will learn how to prepare their organization for trouble-free Part 11 related inspections.
Areas Covered in the Session:
FDA's current inspection and enforcement practices
FDA's new interpretation: learning from FDA inspection reports
Strategy for cost-effective implementation of Part 11: A six step plan
Justification and documentation for the FDA and your management
Who Will Benefit:
QC Managers
QA Managers and Personnel
IT Administrators
Analysts
Regulatory Affairs
Training Departments
Documentation Department
Consultants
Speaker Profile:
Ludwig Huber Ph.D., is the director and editor of Labcompliance the global online resource for validation and compliance. He is the author of the books 'Validation and Qualification in Analytical Laboratories' and 'Validation of Computerized Analytical and Networked Systems, Informa Healthcare'. He has given more than 300 presentations mainly on GLP/GMP, 21 CFR Part 11 and Validation around the world.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
Areas Covered in the Session:
FDA's current inspection and enforcement practices
FDA's new interpretation: learning from FDA inspection reports
Strategy for cost-effective implementation of Part 11: A six step plan
Justification and documentation for the FDA and your management
Who Will Benefit:
QC Managers
QA Managers and Personnel
IT Administrators
Analysts
Regulatory Affairs
Training Departments
Documentation Department
Consultants
Speaker Profile:
Ludwig Huber Ph.D., is the director and editor of Labcompliance the global online resource for validation and compliance. He is the author of the books 'Validation and Qualification in Analytical Laboratories' and 'Validation of Computerized Analytical and Networked Systems, Informa Healthcare'. He has given more than 300 presentations mainly on GLP/GMP, 21 CFR Part 11 and Validation around the world.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
