Annual Product Quality Review - 2017

Overview:
It is designed to minimize the product defects and also the risks associated with the manufacturing of the pharmaceutical product.

Why should you Attend:
This webinar will give a brief overview of the general procedure for the preparation and documentation of the Annual Product Quality Review and also focuses on the regulations and the regulatory requirements as per US and Europe.

Areas Covered in the Session:

•     Discuss how to write APRs
•     Outline the requirements for APR reporting
•     Review what information to include in the reports
•     Discuss how well written APRs benefit your firm's compliance

Who Will Benefit:

•     Site Quality Operations Managers
•     Quality Assurance personnel
•     Plant Managers and Supervisors
•     Manufacturing Superintendents and Managers
•     Regulatory Affairs Managers

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.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

Others Details

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