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.
WHY SHOULD YOU ATTEND?
This webinar will 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.
AREA COVERED
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
LEARNING OBJECTIVES
- 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?
Quality Assurance/Quality Control Directors, Managers, and Specialists
Regulatory Affairs/Regulatory Compliance Directors, Managers, and Specialists
Engineering/Development Directors, Managers, and Specialists
This webinar will 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
- 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
Quality Assurance/Quality Control Directors, Managers, and Specialists
Regulatory Affairs/Regulatory Compliance Directors, Managers, and Specialists
Engineering/Development Directors, Managers, and Specialists
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. Prior to this role, Danielle 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. Danielle began her QA career as a Quality Control Pharmaceutical Microbiologist at a contract laboratory where she performed various tests for their clients. In the years after, she …
Upcoming Webinars

Managing Toxic & Other Employees Who Have Attitude Issues


Stress, Change And Team Resilience Through Humor: An Intera…


The Importance of the first 5 seconds when presenting

Excel Power Skills: Master Functions, Formulas, and Macros …


Unlock Employee Loyalty: Stay Interviews Will Keep Them Eng…


Female to Female Hostility @Workplace: All you Need to Know

The Monte Carlo Simulations in Excel for Risky Investments

Cleaning Data without Complex Functions - A Course for Data…

How to Give Corrective Feedback: The C.A.R.E. Model - Elimi…


Excel - Lists and Tables - A Beginner's Guide to Managing L…

6-Hour Virtual Seminar on Learning the Highlights of Excel …

Interactive dashboards & analytics in Excel



ChatGPT and Project Management: Leveraging AI for Project M…


Excel - Pivot Tables - The Key To Modern Data Analysis and …


Leadership: Strategic Planning and Decision Making

Retention Starts Here: Stop Losing Your Critical Talent and…