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We are holders of GLP certificate since 2014. Since then, we have conducted many residue and pharmacokinetic studies for external partners. Also for our own needs during VMP registrations. Tekrolab experience is growing quickly.
Our facilities are being regularly inspected by Czech State Institute for Drug Control.
All studies with Tekrolab experience are conducted to ensure maximum animal welfare and to avoid unnecessary suffering in accordance with the Directive 2010/63/EU of the European Parliament and of the Council of 22 September 2010 on the protection of animals used for scientific purposes.
Tekro’s journey as a veterinary drug manufacturer has started already in 2003. During that time, we have finally built a strong position in Veterinary Industry in Europe having 45 of our own VMP registered.
We specialize mainly on peroral formulations, feed water medications and medicated premixes in particular. Our production proceeds in accordance with the GMP principles. It is acknowledged by regular inspections from Czech Institute for State Control of Veterinary Biologicals and Medicines.
We are holders of GMP certificate, License for the production of veterinary medicinal products and License for the distribution of veterinary medicinal products.
13 pre-clinical studies with various animal species conducted in accordance with GLP principles
45 VMPs with more than 12 APIs registered in Czech Republic, Slovakia, Hungary and Ukraine.
Pharmacovigilance services currently provided to several marketing authorisation holders.
More than 20 years of experience in regulatory affairs and close contact with European competent authorities.
