In this webinar you will learn about the types of FDA inspections, preparations such as assigning personnel to specific tasks for the FDA 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 techniques for responding to 483s and warning letters. 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 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 an FDA warning letter.

AREAS COVERED

• Personnel preparation

• Procedure to follow during FDA audits -what to do/ what not to do

• Facility requirements to support FDA inspection

• Behavior during inspection-what not to sign

• Internal/ mock audits

• 483s/ FDA Warning Letter response

LEARNING OBJECTIVES

Learn how to handle an FDA inspection efficiently. Also learn effective strategies to avoid 483s as well as for responding to an FDA warning letter.

WHO WILL BENEFIT

• Engineering personnel

• Engineering management

• Quality/ regulatory Management

• Corporate Management

• Manufacturing Management

• Division management

• Legal counsel

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