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EVENT DATE
Dec 2015
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Handling OOS Test Results and Completing Robust Investigations

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Overview

This training program will describe when a full investigation should be triggered and the frequency for re-testing and re-sampling. Attendees will also learn how to implement corrective and preventive action plans (CAPA).

Why Should You Attend:
This 60-minute accredited course is designed to provide sound training on how to recognize and investigate atypical or out of specification results, using approaches which have been recommended by regulatory authorities, performing appropriate investigations.

Who Will Benefit:
Lab analysts
Supervisors and managers in pharmaceutical or biological laboratoriesRegulatory affairs
GMP auditors
Quality control and quality assurance personnel responsible for generating or evaluating test results in a regulated environment
Consultants
Training departments

Instructor Profile:
Danielle DeLucy, MS, is currently an independent consultant to the biologics and pharmaceutical industries specializing in the areas of quality assurance and quality systems. Prior to this role, Ms. DeLucy 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.

Note:
Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2016.

For Registration:
http://www.complianceonline.com/handling-oos-test-results-and-completing-robust-investigations-webinar-training-704351-prdw?channel=eventsinamerica

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