- TypeWebinar
- Location Aurora, Colorado, United States
- Date 26-03-2019
Education/Teaching/Training/Development
Biotechnology
Medical/Healthcare/Hospital
OVERVIEW
In this webinar you will learn about the types of FDA inspections, preparations such as assigning personnel to specific tasks for the inspection, facility requirements to support the inspection (front room, back room), the value of mock audits, how personnel should conduct themselves during the inspection, the inspection process and responding to 483s and FDA warning letter.
How to respond and when is critically important.
Also covered will be the FDA’s rights during the inspection and documentation you are not required to show them.
WHY SHOULD YOU ATTEND
FDA is required to conduct an inspection every two years. A company that is prepared for FDA audits 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 an FDA warning letter.
AREAS COVERED
LEARNING OBJECTIVES
Learn how to be always prepared for FDA inspections and how to handle 483s and FDA warning letter. Also understand the significance of mock audits.
WHO WILL BENEFIT
Use Promo Code MKT10N and get flat 10% discount on all purchases
For more detail please click on this below link:
https://bit.ly/2Nn7MSJ
Email: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882
Know how to prepare your organization for FDA inspections and how to handle the FDA audits. Also learn about the types of FDA inspections and the significance of mock audits.
Training Doyens 26468 E Walker Dr, Aurora, Colorado 80016
+1-720-996-1616