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 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:
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:
Quality Assurance/Quality Control Directors, Managers, and Specialists
Regulatory Affairs/Regulatory Compliance Directors, Managers, and Specialists
Engineering/Development Directors, Managers, and Specialists
Danielle DeLucy 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 …
The Importance Of Documentation For Supervisors And Managers
Project Management for Non-Project Managers - How to commun…
Stop Letting that Difficult Person Ruin your Day - Effectiv…
Nailing the Candidate Experience, Attracting Talent
FDA's Technology Modernization Action Plan (TMAP) And Impac…
Supervising a Human Error Free Environment: You can do a Lo…
Developing and Implementing Inclusive Leadership Strategies
Improving Organizational Performance through Enhanced Emplo…
Creative Leadership through Emotional (EQ) and Humor (HQ) I…
FDA's new Cosmetic labeling requirements
New Announcement! DHS Terminates The I-9 Form Remote Option…
Faster Payments in Today's World - Details on the Different…
Why EBITDA Doesn't Spell Cash Flow and What Does
Payroll Management - Tips To Make Payroll Processing Easier…
Ultimate Persuasion Strategies! - Secret Influence Tools & …
Small Business Management Made Simple: Tools, Tips & Techni…
Introduction to Design of Experiments
Design Control for Medical Devices and Combination Products
I-9 Audits: Strengthening Your Immigration Compliance Strat…
Accounting For Non Accountants : Debit, Credits And Financi…
Employee Business Expense Reimbursement (2023 Updates)
Project Management for administrative professionals
Managing Toxic & Other Employees Who have Attitude Issues
Establishing Appropriate Quality Metrics and Key Performanc…
Onboarding is NOT Orientation - How to Improve the New Empl…
Harassment, Bullying, Gossip, Confrontational and Disruptiv…