FDA Inspections: What Regulations Expect
OVERVIEW
In this 90 minute webinar attendees will gain an understanding of the parameters, approaches, and concerns of FDA inspectors, and the tools for preparing, coping, and managing those inspections in the pharmaceutical, biologics, and med device facilities. Other objectives include inspection authorities and processes including 483s, warning letters, recalls, and other potential actions, inspection processes, use of mock audits required documentation, formats, archiving, as well as how to respond to inspection and audit results.
WHY SHOULD YOU ATTEND
One should attend this webinar to increase one’s knowledge of FDA inspections, what inspectors are looking for and expect to see and not to see in manufacturing facilities. One will gain a better understanding of the parameters, approaches, and concerns of FDA inspectors. One will also gain a more in depth understanding of how to prepare for unannounced FDA audits and inspections.
AREAS COVERED
- The inspection Process
- Legal Issues
- Inspection Checklists
- Part 11 Signatures
- Archiving
- Audit Trails
- Mock Audits
- Documentation
- Report Writing
- Responding to FDA 483’s
WHO WILL BENEFIT
- Quality Assurance Managers and Supervisors
- Validation managers and Supervisors
- Engineering Managers and Supervisors
- Regulatory Affairs Managers and Supervisors
- Manufacturing and Operations managers and Supervisors
- Laboratory managers, supervisors and analysts
- IT managers and staff
- Consultants
- Senior quality managers
- Validation engineers
- Manufacturing engineers
- Production engineers
- Design engineers
- Process owners
- Quality engineers
- Quality auditors
LEARNING OBJECTIVES
Attending the webinar will give you a thorough understanding of the expectations and procedures of FDA inspectors. It will help you understand and devise strategies to be prepared for and manage inspections in manufacturing facilities.
For more detail please click on this below link:
Email: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882
Speaker and Presenter Information
Upon earning a degree in Zoology at North Carolina State University, Joy McElroy made her debut in the pharmaceutical industry in 1992 at Pharmacia & UpJohn performing environmental monitoring and sterility testing. Her hard work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw their quality control lab. In 1998, Ms. McElroy moved to Wyeth Lederle and worked in quality assurance, performing GMP compliance audits, batch record reviews, and holding annual GMP training for new employees. After working in quality assurance for a few years, she moved into equipment qualification and cleaning validation at Mallinckrodt.
Relevant Government Agencies
Dept of Health & Human Services
View Exhibitor/Sponsorship Details
Event Type
Webcast
When
Wed, Dec 13, 2017, 1:00pm - 2:30pm
ET
Website
Click here to visit event website
Event Sponsors
Organizer
Training Doyens