Introduction
In the pharmaceutical industry, quality isn’t a one-time event—it’s a continuous process. An Annual Product Quality Review (APQR) is a regulatory-mandated activity that evaluates the consistency and performance of drug products over time. It helps ensure that each product maintains its intended quality throughout its lifecycle.
What Is APQR?
APQR involves a comprehensive, yearly review of manufacturing and control data associated with a particular product. It is required by regulatory bodies like the USFDA (21 CFR Part 211.180(e)) and EMA (EU GMP Chapter 1), and is a key element of a robust Pharmaceutical Quality System (PQS).
Key Elements of APQR
Why Is It Important?
Conclusion
At apicule, we offer expert support in compiling and reviewing APQRs, helping pharmaceutical companies stay compliant, improve quality, and maintain patient trust—year after year.
Pharmaceutical drugs must maintain their potency, safety, and effectiveness throughout their shelf life. Analytical development plays a critical role in assessing and ensuring drug formulation stability. Importance of Analytical Development... Read more
IntroductionBringing a pharmaceutical product to the U.S. market requires more than innovation—it demands precise and compliant FDA regulatory filings. From early development to commercial approval, the FDA review process is... Read more
Pharmaceutical products must meet strict regulatory requirements to ensure their safety, efficacy, and quality. Analytical testing plays a crucial role in maintaining compliance with these regulations by verifying the chemical... Read more