A fully accredited pharmaceutical testing facility in Oirschot — equipped for quality control, microbiology and stability studies for both veterinary and human pharmaceutical products.
Our laboratory operates under strict GMP and ISO standards, providing pharmaceutical companies across Europe with reliable, independent testing services. Whether you need routine batch release analysis or complex method validation, our team of analytical chemists and microbiologists is ready.
Explore each area of our laboratory and discover the capabilities and equipment available to support your project.
Our analytical chemistry area houses HPLC, GC, UV/Vis spectrophotometry and ICP-OES instruments. We perform identity, assay, related substances and dissolution testing to Ph.Eur. and USP standards — supporting both method development and routine release testing.
Our analytical chemistry suite is equipped with HPLC, GC, ICP-OES, UV/Vis and Karl Fischer instrumentation — covering the full range of physicochemical testing required for pharmaceutical batch release and development.
Our dedicated, ISO-controlled microbiology suite operates with laminar flow cabinets, incubators and aseptic workstations. All testing is performed to current Ph.Eur. standards by our qualified microbiologists.
Quality assurance is not just something we test — it's something we practice. Our laboratory holds a Manufacturing and Import Authorisation (MIA) and operates in full compliance with EU Good Manufacturing Practice.
Issued under EU GMP regulations, our JMP certificate confirms that the Regivet laboratory in Oirschot meets all requirements for the manufacture and import of veterinary and human pharmaceutical products. MIA numbers: 2924-F (veterinary) and 109627 F (human).
Our laboratory team is available to assess your testing requirements and provide a tailored proposal — typically within 2 working days.