Driving Innovation: Contract Research for Breakthrough Discoverie

Contract

research

Contract

research

GLP studies designed for regulatory success

We provide GLP – compliant studies tailored to human and veterinary medicinal products.

Our expertise covers:

Pharmacokinetics & bioavailability

In vivo and in vitro bioequivalence studies

Residue depletion studies

Safety & tolerance studies

Analytical method development

Feed and nutritional studies

Clinical trials in cooperation with Czech farms and breeders

From protocol design to final report, we ensure regulatory acceptance (EMA, EFSA).

The GLP testing facility in Dětřichov:

6 independent sections
group and individual stabling
controled ventilation in each section

We can stable multiple animal species:

Pigs (up to 720 pieces of pigs)

Cattle (up to 40 pieces of cattle)

Sheep and goats (up to 192 pieces of sheep and goats)

Broilers and laying hens (up to 5760 pieces of broilers and laying hens)

Turkey (up to 780 pieces of turkey)

We are here for

Human and veterinary pharmaceutical companies
Scientific and Research organizations

Universities and public institutes
Feed additive suppliers

We are here for

Human and veterinary pharmaceutical companies
Scientific and Research organizations

Universities and public institutes
Feed additive suppliers

Comprehensive GLP & GMP Analytical Services for Pharma and Veterinary Products

Our analytical laboratory provides high-quality services in regulated GLP and GMP environment. The laboratory offers:

LC, LC-MS method development and validation

Infrared spectroscopy, Atomic absorption spectroscopy

Development, validation, verification and transfer of chromatographic, spectral and titration method according to ICH/VICH.

VMP release testing by Qualified Person (QP)

VICH Stability studies

Let’s work together …

Initial consultation with our experts – objectives, timelines, and regulatory requirements to define the study scope.
Project proposal – Detailed study plan including methodology, schedule, and budget.
Study protocol and approvals – GLP-compliant protocol design and securing ethical and authority approvals.
Study execution – Animal housing, dosing, sampling and laboratory analyses under strict quality and welfare standards.
Data management and statistical analysis – detailed examination of results
Reporting – Comprehensive final report prepared for regulatory submission.

Certification

GLP

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.

GMP

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.

Our experts