Event Location

Neighborhood: Upper West Side

Online Event

161 Mission Falls Lane, Suite 216

Fremont, CA 94539


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

Start on : June 21, 2017 10:00 AM Wednesday
End on : June 21, 2017 11:00 AM Wednesday

Event Details

Annual Product Quality Review (APR) is an evaluation conducted annually to determine if there are any possible changes in the process or manufacturing of the pharmaceutical product or any change in the specifications of the product or any change in the manufacturing process.

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: support@compliance4All.com

People Attending Annual Product Quality Review - 2017

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