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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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April 12, 2017 |
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Compliance4All, Online
2017-06-21
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
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
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Organized by:
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Compliance4All |
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Invited Speakers:
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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.
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Deadline for Abstracts:
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2017-06-20
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Registration:
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Full Details & Registration Link: http://www.compliance4all.com/control/w_product/~product_id=501335LIVE?channel=bio-mirror_Jun_2017_SEO
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E-mail:
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support@compliance4All.com
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