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 any change in the specifications of the product or any change in the manufacturing process. It is designed to minimize product defects and the risks associated with the manufacturing of pharmaceutical products.
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 in per US and Europe. It will also discuss the comparative evaluation of similarities and differences in 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.
AREA COVERED
- Annual Product Review definition
- What details need to be included in the report?
- A model of an example Annual Product Review Report
- Review of Citations
LEARNING OBJECTIVES
- Discuss how to write APRs
- Outline the requirements for APR Reporting
- Review what information needs to be included in the reports
- Discuss how well-written APRs benefit your firm’s compliance
WHO WILL BENEFIT?
- Quality Assurance Teams
- Compliance Teams
- Regulatory Affairs Teams
- Quality Assurance/
- Quality Control Directors,
- Managers, and Specialists
- Regulatory Compliance Directors
- Engineering/Development Directors
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