Annual Product Quality Review - 2017

Overview:
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