FDA vs EU Inspections - Getting Prepared and What are Differences | January 27, 2016 10:00 AM - January 27, 2016 1:00 PM | Automation.com

FDA vs EU Inspections - Getting Prepared and What are Differences

Event Summary

DATE:
January 27, 2016
START DATE/TIME:
January 27, 2016 10:00 AM
END DATE/TIME:
January 27, 2016 1:00 PM
EVENT TYPE:
Training
HOST:
Online Compliance Panel
PHONE:
15108575896
EMAIL:
[email protected]
WEBSITE:
Click here to Visit

Description

Description

This training is a comparative look at FDA & EU regulations to help attendees understand the FDA and EU inspection process and how to prepare for both of them. Attendees will learn the best practices to respond to Form 483 citations, Warning Letters and EU inspection findings.

Objectives of the Presentation

Differences between FDA and EU Inspections including the FDA and EU joint inspection programmer
How to prepare for EMA and FDA audit
How to plan for an audit or inspection using checklists/FDA/EMEA inspection guidelines
Tips for employees before the inspection
Tips on proper responses to prepare for audit/inspection Interviews
Setting up a Triage to ensure that required documents are available
How to interact with the inspectors-Dos and Don'ts
How to reply to inspection reports, 483's and EU inspection finding
Post inspection actions - implementing appropriate CAPAs in response to audit findings

Why Should you Attend

FDA and EU GCP regulations and standards apply pharmaceuticals, biologics and medical devices. Failure to conform to these requirements may result in concerns about quality and integrity. Inspections are critical to the success of business on several levels. Therefore, being appropriately prepared and management of the inspection and audit process are critical activity. The consequences if a company does not pass an inspection are time consuming, delayed product approvals, and could lead to civil or even criminal litigation by the FDA and EU inspection agencies.

This webinar has been specifically designed to help attendees prepare for FDA and EU inspection. It will provide a background and understanding of the role played by the regulatory inspectors, and the administrative and enforcement powers. Attendees will be taken through the key stages of FDA and EU inspection processes and understands the various types of inspections that can be carried out.

Who can Benefit

Quality Assurance Managers and Auditors
Regulatory Affairs
Document Management
Other professionals who want to know more about inspection guidelines

Note: Use Promo code SMEVB and get 10% off on registration (Valid till Jan 31st)

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