Isoquimen, SL works in a regulated GLP environment covering the process and the conditions under the non-clinical studies are planned, performed, monitored, recorded, reported and archived.
Isoquimen, SL has over 10 years of experience in the performance of GLP studies with human and veterinary drugs. We are certified by the health authorities to work under Good Laboratory Practices (GLP) and we are periodically inspected as part of the compliance program of the GLP.