Time: March 26, 2019 from 1pm to 2pm
Location: Training Doyens 26468 E Walker Dr,Aurora, Colorado 80016-6104
Street: 26468 E Walker Dr,Aurora, Colorado
Website or Map: https://bit.ly/2TY3NPi
Event Type: online
Organized By: Training Doyens
Latest Activity: Feb 22, 2019
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.
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:
Toll Free: +1-888-300-8494