The purpose of quality assurance (QA) in public pharmaceutical supply systems is to make certain that each medicine reaching a patient is safe, effective, and of standard quality. QA activities in the pharmaceutical industry should be comprehensive, spanning the entire supply process from medicine selection to patient use.
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Pharmaceutical Quality Control Procedures
Pharmaceutical quality control testing is usually a matter of repetitive testing of samples of APIs or of a limited number of pharmaceutical products, whereas national quality control laboratories have to be able to deal with a much wider range of pharmaceutical substances and products and, therefore, have to apply a wider variety of test methods. Specific recommendations for national pharmaceutical quality control laboratories are addressed in the following text. Particular consideration is given to countries with limited resources wishing to establish a governmental pharmaceutical quality control laboratory, having recently done so, or which are planning to modernize an existing laboratory.
Quality control laboratories may perform some or all quality control activities, e.g. sampling, testing of APIs, excipients, packaging materials and/ or pharmaceutical products, stability testing, testing against specifications and investigative testing.
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