FDA Inspection and Respond to 483 & How to Prepare them - 2017
In this webinar you will learn about the types of FDA inspections, preparations such as assigning dedicated personnel to specific tasks for the inspection, facility requirements to support the inspection.
Why should you Attend:
FDA is required to conduct an inspection every two years. A company that is prepared for the inspection is less likely to receive 483's than a disorganized company. If a 483 is received knowing how to respond will lessen chances of receiving a Warning Letter.
Areas Covered in the Session:
- Personnel Preparation
- Facility needed to support inspection
- Behavior during inspection-what not to sign
- Internal/ Mock audits
- 483 response
Who Will Benefit:
- Engineering Personnel
- Engineering Management
- Quality Management
- Corporate Management
- Manufacturing Management
- Division Management
Speaker and Presenter Information
Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis and software validation for the past 8 years.
Relevant Government Agencies
FDA
Event Type
Webcast
This event has no exhibitor/sponsor opportunities
When
Tue, Aug 8, 2017, 10:00am - 11:00am
PT
Cost
| Live Webcast: | $150.00 |
| Recorded Webcast: | $190.00 |
Website
Click here to visit event website
Organizer
NetZealous - Compliance4All
