Quality compliance​

BioAdvice has an authorization from the Danish Medicines Agency to perform preclinical pharmacological studies, toxicological studies, and a wide range of laboratory analyses according to GLP. Furthermore, the company is experienced in running batch release tests (BP/USP) according to GMP. In addition to these studies, many non-GLP studies are also performed in the same quality assured environment.

Write to BioAdvice​

Please make sure all required fields are filled out correctly

BIOADVICE A/S - Lyshoejvej 21, DK-3650 Oelstykke, Denmark - Tel: +45 38 25 20 15 - E-mail: bioadvice@bioadvice.dk - CVR: 25052927


Lyshøjvej 21, 3650 Ølstykke

Tel: +45 35 25 20 15

E-mail: lm@bioadvice.dk

CVR: 25052927