3-Hour Virtual Seminar on FDA's New Enforcement of 21 CFR Part 11
This 3 hour Virtual seminar will explain about FDA's current inspection and enforcement practices , and also explain how to prepare your company for Part 11 Inspections.
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FDA continues to enforce Part 11 through its ongoing Part 11 inspection and enforcement program. Just in the last 3 years FDA issued more than 30 warning letters with Part 11 related observations. Citations are related to inadequate integrity, security and availability of electronic records, including data manipulation.
There are many questions about the ongoing inspection and enforcement program, e.g., what inspectors are looking at, what are major findings and what are the FDA expectations about follow up.
The seminar will have the answers. And 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.
Why should you Attend:
There are many questions about the P11 inspection program, e.g., what inspectors are looking at and what major findings are. The seminar 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.
Failing Part 11 and data integrity inspections can have a high negative impact on regulated companies, on individual employees and most important on the health and safety of the consumers of products such as drugs and medical devices.
- publications of FDA Warning Letters will have a negative impact on the company's impact
- shipment stops resulting in loss of revenues and profit
- product recalls
- import alerts
- consent decrees
- requirements for extensive corrective and preventive actions
- requirement for hiring 3rd party consultant
While the Part 11 regulation is spelled out very clearly and is well understood by regulated companies, FDA inspections are not. Regulations such as Part 11 and GMPs set forth minimum requirements to assure that drugs meet the standards of the Federal Food, Drug, and Cosmetic Act (FD&C Act) regarding safety, identity, strength, quality, and purity. Frequently inspectors ask more because regulations are subject to inspector's interpretations and somewhat unpredictable and sometimes come as a surprise.
The seminar will come with and discuss more than 20 typical inspectional observations and give recommendations on how to avoid observations.
And most important: Attendees will have the unique opportunity to ask life questions to the Part 11 and Data Integrity expert during and at the end of the seminar.
Areas Covered in the Session:
Who Will Benefit:
- FDA's past inspection and enforcement practices
- Reason for changing inspections and enforcement
- FDA's new interpretation: learning from FDA inspection reports
- How can the new requirements be implemented in your company
- 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 and Data Integrity Inspections
- The importance of the quality management system (QMS) and global corporate for Part 11 and data integrity
- Questions and answers
- Sharing best practices
- IT Managers and System Administrators
- QA Managers and Personnel
- Validation Groups
- Software Developers
- Validation Professionals
- Training Departments
- Documentation Department
- IT and GMP Consultants
- Personnel from Pharma, Biotech and Medical Device Industries