Seminar
Seminar on Why is FDA at my Facility, and what do I do During an Inspection
Biology · Life Sciences · Food Industry
Key numbers
- Editions on record
- 1first in 2016
About Seminar on Why is FDA at my Facility, and what do I do During an Inspection
Course "Why is FDA at my Facility, and What do I do During an Inspection" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer.
From our listing of this edition. Details may have changed since.
Editions
| Year | Dates | Where | Exhibitors | Visitors |
|---|---|---|---|---|
| 2016 | 18–19 Jul 2016 | — | — |
Past editions from the bvents archive (2008–2019) and organiser figures where they were published.
Questions
When is Seminar on Why is FDA at my Facility, and what do I do During an Inspection?
The next dates haven't been confirmed. The last edition we have on record was 18–19 Jul 2016.