FDA's New Enforcement of 21 CFR Part 11 - Recorded Webinar

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Robinson
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Webinar Duration: 75 minutes

RECORDED: Access recorded version only for one participant; unlimited viewing for 6 months (Access information will be emailed 24 hours after the completion of payment)

SPEAKER: Ludwig Huber

OVERVIEW:
FDA continues to enforce Part 11 through its new Part 11 inspection and enforcement program. Just in the last 3 years, FDA issued more than 30 warning letters with Part 11 violations. Citations are related to inadequate integrity, security and availability of electronic records but also related to validation of software and computer systems. There are many questions about the program, e.g., what inspectors are looking at what are major findings.

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
- Going through case studies from laboratories, offices and manufacturing with graphical workflow of records, step-by-step description, recommendations for individual Part 11 requirements with justifications and documentation for the FDA and your management
- Case studies how to avoid or respond to Part 11 related observations with corrective actions to fix current issues and preventive actions to prevent reoccurrence of the same or similar issues
- How to prepare your company for Part 11 Inspections

For Easy Implementation, Attendees Will Receive:
- Checklist: Part 11 compliance
- Case Studies: How to avoid Part 11 related 483's and Warning Letters
- SOP: Electronic Audit trail: Specifications, Implementation, Validation

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. For more information, please visit Dr. Huber’s website www.ludwig-huber.com

After your payment, we will contact you with instructions about how to access the webinar.
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