Understand the terms behind the science

C Competitive Antagonist A competitive antagonist competes with an agonist for the same receptor-binding site, and its effect can generally be overcome by increasing the agonist concentration. Competi... Read definition → C Contamination Contamination is the unintended introduction or presence of chemical, physical, or microbiological impurities in a material, product, or environment. Contamination হলো কোনো ma... Read definition → C Content Uniformity Content uniformity is the assessment of whether individual dosage units contain the amount of active ingredient required by the applicable specification. Content Uniformity te... Read definition → C Controlled-Release Dosage Form A controlled-release dosage form is designed to release a drug according to a predetermined release pattern over a specified period. Controlled-Release Dosage Form এমনভাবে তৈর... Read definition → C Corrective and Preventive Action (CAPA) A system for correcting identified problems, addressing their causes, and preventing their recurrence or occurrence. চিহ্নিত সমস্যা সংশোধন, সমস্যার কারণ মোকাবিলা এবং পুনরাবৃত্... Read definition → C Cracking Cracking is the formation of visible cracks on the surface or within the body of a tablet. Cracking হলো tablet-এর surface অথবা ভেতরে দৃশ্যমান ফাটল সৃষ্টি হওয়া। এটি formulation... Read definition → C Cream A cream is a semisolid emulsion-based preparation intended for application to the skin or certain mucous membranes. Cream হলো emulsion-ভিত্তিক একটি semisolid preparation, যা স... Read definition → C Critical Process Parameter (CPP) A Critical Process Parameter is a process variable whose variability can affect a critical quality attribute and therefore must be monitored or controlled to ensure the desire... Read definition → C Critical Quality Attribute (CQA) A Critical Quality Attribute is a physical, chemical, biological, or microbiological property that must remain within an appropriate limit, range, or distribution to ensure th... Read definition → C Cross-Contamination Cross-contamination is the unintended transfer of a substance or contaminant from one material, product, or process to another. Cross-contamination হলো একটি material, product ... Read definition → D Deliquescence Deliquescence is the process in which a solid substance absorbs sufficient moisture from the atmosphere to dissolve in the absorbed water and form a solution. Deliquescence হল... Read definition → D Design of Experiments (DoE) Design of Experiments is a structured statistical approach for studying how multiple factors influence a process or product response. In pharmaceutical development, DoE can he... Read definition → D Deviation A departure from an approved instruction, established procedure, specification, or standard. অনুমোদিত নির্দেশনা, প্রতিষ্ঠিত procedure, specification বা standard থেকে বিচ্যুতিক... Read definition → D Diluent A diluent, also called a filler, is an excipient added to increase the bulk of a formulation when the quantity of active ingredient alone is insufficient for convenient manufa... Read definition → D Disinfection Disinfection is a process used to eliminate or reduce harmful microorganisms on inanimate surfaces, although it may not destroy bacterial spores. Disinfection হলো জড় পৃষ্ঠে ক্... Read definition → D Disintegrant A disintegrant is an excipient that promotes the breakup of a tablet or capsule contents into smaller particles after contact with a suitable liquid. Disintegrant হলো এমন একটি... Read definition → D Disintegration Disintegration is the breakdown of a solid dosage form into smaller particles or fragments under specified conditions. Disintegration হলো নির্দিষ্ট পরীক্ষার শর্তে tablet বা ca... Read definition → D Disintegration Test A disintegration test determines whether a tablet or capsule breaks down within a specified time under prescribed test conditions. Disintegration Test-এর মাধ্যমে নির্ধারিত পরী... Read definition →