What is Dissolution Testing? Dissolution testing measures how quickly and completely a drug dissolves in a particular solvent. The United States Pharmacopeia (USP) standard for dissolution testing, known as USP <711>, provides guidelines to ensure…
The West African Health Organization (WAHO) has adopted the Common Technical Document (CTD) format to standardize the registration of pharmaceutical products across the Economic Community of West African States (ECOWAS). This format helps pharmaceutical companies…
The International Council for Harmonisation (ICH) is a global organization that plays a key role in ensuring that medicines are safe, effective, and high quality. It brings together regulatory authorities and the pharmaceutical industry from…
The Drug and Related Product Labelling Regulations, 2021, introduced by Nigeria’s National Agency for Food and Drug Administration and Control (NAFDAC), lay down the rules for the labeling of drugs and related products. These regulations…
Quality Control in Medicinal Products | Quality Control Principle | Quality Control General Information | Good Quality Control Laboratory Practice | Play Video Inside the Pharmaceutical Quality Control Department: Ensuring Safety and Efficacy Quality Control…
