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 Abbreviated New Drug Application (ANDA) is the regulatory pathway for getting generic drugs approved by the U.S. FDA. Filing an ANDA is a strategic move that allows pharmaceutical companies...
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...
IntroductionFormulation development is the science of designing and optimizing a drug product’s composition to ensure therapeutic effectiveness, safety, and patient compliance. Whether it's a tablet, injectable, cream, or capsule, every...