OOS Test Results and Completing [Robust] Investigations

MessageThis Webinar is over
Date Nov 30, 2018
Time 10:00 AM to 11:30 AM
Cost 150.00
Online
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 90-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.

Areas Covered in the Session:
Developing a Proper CAPA Plan to Address Any Corrective Actions
How to Properly Document Findings
Example of a Proper OOS Investigation Write Up

Who Will Benefit:
Lab Analysts
Supervisors and Managers in Pharmaceutical or Biological Laboratories
Regulatory Affairs
GMP Auditors
Consultants
Training Departments

Speaker Profile:
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 17 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

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

 


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