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Quality matters!

Quality is embedded in everything we do. Wieslab is accredited according to ISO 17025 and is compliant with GLP. A key part of our quality work is to constantly develop the laboratory┬┤s technical and scientific expertise.

GLP laboratory

Wieslab has since May 2015 been part of Swedac program of Good Laboratory Practice (GLP) as STAFS 2008: 4 Swedac regulations imposing OECD principles on the introduction of Good Laboratory Practice (GLP), the European Directives 2004/9 / EC and 2004/10 / EC and OECD. Wieslab GLP approved to perform bioanalytical testing in non-clinical safety studies of drugs (Analytical and Clinical Chemistry Testing).

Click here GLP statement from SWEDAC.

Wieslab also performs bioanalytical testing for clinical drug trials according to EU directives 2001/20 / EC, FDA Title 21 part 58 (21CFR58), and EMA / INS / GCP / 532137/2010 Reflection paper for laboratories That perform the analysis or evaluation of clinical trial samples.

ISO 17025 Accredited laboratory

Wieslab was one of the first private laboratories accredited by SWEDAC and currently works for ISO / IEC 17025: 2005 to fulfill the Sweden and the EU┬┤s high standards for laboratories. The overall objective of the operation is to offer laboratory and clinically working physician a service with fast and reliable decision-making basis for the treatment of autoimmune diseases.

Click here for the 1502 ISO / IEC 17025 accreditation certificate from SWEDAC.

The majority of Wieslabs tests are accredited. Contact us for a list of accredited tests.

GLP certificate
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