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OOS Test Results and Completing [Robust] Investigations

 
  September 28, 2018  
     
 
Netzealous LLC DBA - Compliance4All, Online
2018-11-30


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

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
 
 
Organized by: Event Manager
Invited Speakers:

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.
 
Deadline for Abstracts: 2018-11-29
 
Registration: https://www.compliance4all.com/control/w_product/~product_id=502162LIVE?channel=hum-molgen_Nov_2018_SEO
E-mail: support@compliance4All.com
 
 
   
 
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