Skip to NavigationSkip to content

21 CFR Part 11: How to Successfully Prepare for and Host an FDA Inspection - Primer for Success

Wednesday, August 24, 2011
Online Webinar
Houston, United States

Event Type: Training Course


 Bookmark    Add To calendar

 Short and quick overview of the Part 11 regulation; detailed description of HOW TO prepare for an FDA inspection when and where Part 11 is in scope or the scope of the inspection; detailed description of HOW TO handle the FDA inspection during the inspection itself; some trends when it comes to Part 11 inspections; commonly asked questions; warnning letters examples; and what the future holds when it comes to Part 11.

Why Should You Attend: 

Technical Document : Attendees will receive 30+ commonly asked questions; 21 CFR Part 11 regulation; Sample internal/external audit/inspection checklist based on 21 CFR Part 11 regulation

Who Will Benefit:

Quality Managers.   Quality Engineers.   Small business owners.   Internal and external auditors.   Management Reps.   FDA inspectors.   Consultants.

Areas Covered in the Seminar:

"More and more organizations are striving to ""go green"" and develop ""sustainable"" organization's strategies, which almost always includes using more and more of the computer technologies. Part 11 is a regulation that regulates the technology when it comes to electronic signatures and electronic records and will be more then ever a part of the scope of the FDA inspections, yet most organization do not know how to best prepare for such inspections. In a time of global economy when and where time is of essence, having an ability to access records from any location around the world is more critical then ever, and for the same reason, electronic records will be more needed and desired in each organization. In addition, approval of documents and records in a timely fashion is absolutely needed at all times, and being able to do just that via an electronic media is understood. For both, electronic signatures and electronic records, the organization shall comply with the Part 11 regulation."

Mission Statement is a leading portal for the pharmaceutical industry, providing industry professionals with pharma news, pharma events, pharma service company listings and pharma jobs,
Site content is produced by our editorial team exclusively for and our industry newspaper Pharmafocus. Service company profiles and listings are taken from our pharmaceutical industry directory, Pharmafile, and presented in a unique Find and Compare format to ensure the most relevant matches