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.
By integrating analytical development at every stage of drug formulation, pharmaceutical companies can ensure product stability, efficacy, and regulatory compliance.
IntroductionA robust Quality Management System (QMS) is the backbone of any GMP-compliant pharmaceutical operation. During supplier or vendor audits, evaluating their QMS is essential to ensure that your sourcing partners...
IntroductionFiling a New Drug Application (NDA) is the final and most critical regulatory milestone in the U.S. drug development process. It represents the culmination of years of research, clinical trials,...
When developing analytical methods for pharmaceuticals, two critical aspects must be considered—validation and verification. While both ensure the accuracy and reliability of analytical techniques, they serve distinct purposes. Understanding their...