In this section of GMP-inspection.com, our translators provide definitions and explanations of various specialized terms from the pharmaceutical industry and GMP (Good Manufacturing Practice).
Contamination is the process or condition by which an object, an environment, a product or a surface becomes contaminated or polluted with foreign or undesirable substances, microorganisms, particles or harmful substances. This can happen in undesirable ways and in the context of various fields such as medicine, pharmacy, food processing, research, manufacturing and more.
Contamination can be microbiological (caused by microorganisms such as bacteria, viruses or fungi), chemical (caused by chemicals) or physical (caused by particles or objects that can enter the environment or the product in an undesirable way).
In pharmaceutical production, contamination (German translation: Kontamination) means the undesired introduction of foreign substances, microorganisms or particles into pharmaceutical products or the environment, which can impair the quality, efficacy and safety of the drugs produced. Contamination can occur at various stages of pharmaceutical manufacture and can be microbiological, chemical or physical in nature.
Contamination can be extremely dangerous as it can lead to products being released onto the market that can cause adverse drug reactions, allergies, infections or even serious illness. The pharmaceutical industry has strict regulations and standards for contamination control (German: Kontaminationskontrolle), which stipulate sterile and safe conditions for the manufacture, storage and transportation of drugs.
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