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The study of how the body absorbs, distributes, metabolizes, and excretes drugs, crucial for determining dosages and drug delivery methods.

Regulations that ensure products are consistently produced and controlled according to quality standards, critical for pharmaceutical manufacturing.

A vessel in which biological reactions are carried out, especially for culturing organisms that produce pharmaceuticals.

The method or process of administering a pharmaceutical compound to achieve a therapeutic effect in humans or animals.

A laboratory technique used to amplify DNA sequences, important in genetic drug development and diagnostic testing.

The manipulation and control of matter at the nanoscale, promising new drug delivery methods and treatments in pharmaceutical engineering.

The proportion of a drug that enters circulation when introduced into the body and is able to have an active effect.

A technique for separating chemical substances based on differences in their movement through a material, essential for drug purity testing.

The physical form in which a drug is produced and administered, such as tablets, capsules, or injections, influencing drug delivery and action.

The substance in a pharmaceutical drug that is biologically active, primarily responsible for the drug's desired effects.

The process of eliminating all microbial life, including spores, from a surface or product, essential for ensuring safety in pharmaceutical products.

A controlled environment with a low level of pollutants, used in the manufacturing of pharmaceuticals to prevent contamination.

The study of biochemical and physiological effects of drugs on the body, explaining how a drug exerts its effects.

The process of forming grains or granules from a powdery substance, improving the flow of powder mix during tablet manufacturing.

The process of compacting powder into tablets that can be swallowed, ensuring consistent dosage and drug stability.

A freeze-drying process that removes water from a product, preserving the stability and prolonging the shelf life of pharmaceuticals.

A computational method that predicts the preferred orientation of one molecule to a second, aiding drug design and discovery.

Basic steps in a process, such as distillation, filtration, or crystallization, used in the manufacturing of pharmaceuticals.

A manufacturing method where input materials are continuously fed and products are continuously taken out, increasing efficiency in pharmaceutical production.

The authorization granted by the U.S. Food and Drug Administration for a new pharmaceutical to be marketed, ensuring drug safety and efficacy.

The process of proving that any procedure, process, equipment, material, activity or system leads to the expected and consistent results, crucial in pharmaceutical manufacturing.

The process of increasing batch size or processing volume from laboratory to production scale, a critical step in drug development.

A method of manufacturing where the product is created in stages with intermittent testing, common in pharmaceutical production.

A technique in analytical chemistry used to separate, identify, and quantify components in a mixture, vital for ensuring the purity and potency of pharmaceuticals.