Best Practices for Deviation Investigations

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Presented By 247compliance

Friday, September 27th at 1:00pm EST

Online sale ends: 09/27/19 at 12:00pm EST

247compliance

2035 Sunset Lake, RoadSuite B-2, Newark, Delaware - 19702

Online, DE 19702

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Talent

Danielle DeLucy

Description

OVERVIEW

This webinar will help attendees understand the fundamental steps of a deviation investigation with focus on using documents, interviews, and objective evidence to arrive at a root cause and a corrective and preventative action plan.Learn how to identify and classify deviations for easier management and investigation.

LEARNING OBJECTIVES

Describe what types of deviations exist
Explain how to conduct a proper investigation
Learn new tools for proper root cause analysis
What things to avoid during the investigation
How to properly document and manage the deviation details
How to close the deviation and assess impact to the final product.

WHY SHOULD YOU ATTEND

FDA, EMA, and other international regulatory agencies require that there be a deviation investigation system as a subsystem of a company's overall quality system. Those involved in performing investigations, review and acceptance of non-conformance investigations, will learn how to conduct investigations, dos and don'ts in interviews, how to determine CAPA and more in this webinar.

AREAS COVERED

Review of regulatory requirements for investigations
What is the definition of a Deviation?
Types of Deviations/identification of Deviations
Conducting the investigation
Interviews - dos and don'ts
Source Documents/Evidence
Determining root cause and effective/sustainable CAPA
Key elements of the investigation report

WHO WILL BENEFIT?

Mid-Level Managers
Compliance Officials
Manufacturing Personnel
Laboratory Personnel

SPEAKER

Danielle DeLucy, MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in order to meet Regulatory compliance. Prior to this role, Danielle has been in the industry for 15 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous filling and packaging operations.

For more detail please click on this below link:

http://bit.ly/2krMoSy

Email: support@247compliance.com

Tel: +1-(510)-868-1040

Presented By

Time

1:00pm to 2:30pm
Doors open at 1:00pm

Price

General Admission: $199.00

Age

All Ages

Venue

247compliance<br> 2035 Sunset Lake, RoadSuite B-2, Newark, Delaware - 19702<br> Online, 19702

Info Line

+1-(510)-868-1040