Welcome to the website of TECHPharm GmbH. We are an independent contract laboratory with focus on pharmaceutical industry and perform analytical testing according to the Good Manufacturing Practice (GMP). Our activities are registered at the local authorities (Regierungspräsidium Tübingen, subsidiary Karlsruhe, Germany). Our latest GMP inspection by the Regierungspräsdium Tübingen was completed succesfully on 01. and 03.07.2025. The most recent inspection by the FDA was completed successfully on 07.02. – 09.02.2018.

Our laboratory activities and services focus at pharmaceutical quality control of raw materials, active pharmaceutical ingredients (APIs), auxiliary materials, intermediates, bulk products, finished products and packaging components. In these areas, full testing, parametric testing and microbiological testing according to current pharmacopoeias and specifications are carried out. We furthermore offer method validation, stability testing, process validation, cleaning validation and method development. Stability storage according to ICH is carried out on-site by means of qualified storage rooms and storage cabinets.

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