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Following events are tentatively planned but may be rescheduled, based on CDC guidelines or attendee registration interest .
TENTATIVE: 21 CFR Part 11 Compliance, Boston MA, Sep 22-24, 2021
TENTATIVE: Quality Control Laboratory Compliance, Boston MA, Oct 6-8, 2021
TENTATIVE: Analytical Instrument Qualification and System Validation, Boston MA, Nov 15-17, 2021
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Boston Professional Events List
90 Minutes Live Webinar Annual Product Quality Reviews
Link to Website
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. It is designed to minimize the product defects and also the risks associated with the manufacturing of the pharmaceutical product.
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. It will also discuss the comparative evaluation about similarities and differences of requirements associated with the manufacturing of the drug product in different countries. It is also necessary to know that the regulatory requirements of different countries are different and hence this will further guarantee the quality of the pharmaceutical product.
This webinar will review:
• Annual Product Review definition
• What needs to be included in the report
• A model of an example Annual Product Review Report
• Review of citations
Key Learning Objectives of your Topic:
• 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
The following individuals or disciplines will benefit from attending this Webinar:
Quality Assurance Product Reviewers
Personnel involved in the preparation of the Product Review
Danielle DeLucy, MS, is currently an independent consultant to the biologics and pharmaceutical industries specializing in the areas of quality assurance and quality systems. Prior to this role, Ms. DeLucy has been in the industry for 15 years serving in numerous quality management roles, such as the director of product quality, the oversight of sterility assurance practices and provided QA oversight of numerous filling and packaging operations.
(Contact us : 844-267-7299 | 954-947-5671
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