Medicine

Annual Product Quality Review - 2017

Date 21 June 2017
Location Fremont, United States
Venue Online
Format In Person

About this Conference

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: support@compliance4All.com

Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501335LIVE?channel=confroll_Jun_2017_SEO