As the pace of product development accelerates, the approach to dissolution-method development must advance beyond a manual method and an assay. A natural progression of the method-development process ...

Missed or late calibration dates can accumulate, and even if the equipment is labelled appropriately, it can suggest poor management of resources and priorities. Good manufacturing practice (GMP) ...

an active pharmaceutical ingredient is the active ingredient contained in a drug and it is the basic material with the desired pharmaceutical properties. Active pharmaceutical ingredients play core ...

A fully automated dissolution lab is an integrated, end to end architecture that enables reproducible testing, continuous throughput, and reliable data integrity. Understanding its building blocks, ...

The British Pharmacopoeia on Monday released its response to its consultation on dissolution testing and announced its plans to update its approach within its product monographs. The British ...

Distek, Inc., a leading manufacturer of laboratory testing instruments for the pharmaceutical and biotechnology industry, as well as an experienced provider of validation and qualification services, ...