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About Eurofins BioPharma Product Testing Finland Oy

Eurofins BioPharma Product Testing Finland services encompass R&D & Analytical testing for human and veterinary medicines and manufacturing of investigational medicinal products under GMP.We offer a full range of pharmaceutical product development services from early clinical phases to marketing authorisation, for both human and veterinary products. We conduct stability studies according to the ICH and VICH guidelines, as well as studies tailored to your needs. Our non-sterile expertise spans everything from routine tablet testing to complex inhalation product method development, tailor-made to meet your unique requirements. We are certified in accordance with GMP (Good Manufacturing Practice) and have been operating under a GMP-license since 2005. Our GMP-license also covers manufacture of investigational medicinal products (IMPs) for clinical trials.Our teams of scientists and project managers partner with you throughout the outsourcing process from testing to monthly reports to 24-hour online data access at LabAccess.comSM. In close cooperation with our Eurofins BioPharma Product Testing network of laboratories across Europe, we are able to offer the full service package. Our local presence ensures personalised customer support for all analytical needs.

Locations

Kuopio

Laboratory

Neulaniementie 2, 70210 Kuopio, Finland

Laboratory

+358 20 7670480

sales.fi@bpt.eurofinseu.com

Kuopio

Laboratory

Volttikatu 8, 70700 Kuopio, Finland

Laboratory

+358 20 7670480

sales.fi@bpt.eurofinseu.com

Kuopio

Laboratory

Volttikatu 5, 70700 Kuopio, Finland

Laboratory

+358 20 7670480

sales.fi@bpt.eurofinseu.com

Accreditations

Good Manufacturing Practice Plus (GMP+)

Issuing Body Finnish Medicines Agency (Fimea)

Issuing Body Country n.a.

Issuing Body Website www.fimea.fi/web/en/supervision/good_laboratory_practice_glp_

Good Manufacturing Practice (GMP)

Issuing Body Finnish Medicines Agency (Fimea)

Issuing Body Country n.a.

Issuing Body Website www.fimea.fi/web/en/supervision/good_laboratory_practice_glp_