Annual Product Quality Review - 2017

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Category Annual Product Quality Review, Manufacturing, Risk, Pharmaceutical Webinars, manufacturing technology, industrial manufacturing, industrial manufacturing industry, Regulatory Affairs Managers

Deadline: June 18, 2017 | Date: June 21, 2017

Venue/Country: Online, U.S.A

Updated: 2017-04-24 18:47:15 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com