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.
IntroductionAn unexpected FDA inspection can either validate your compliance efforts—or expose costly gaps. Being prepared is not just about documentation; it’s about building a culture of continuous compliance across your...
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,...
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...