We’re exhibiting at CPHI Frankfurt, 28-30 October 2025     Stand#6.1F83

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Facilities

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Facilities

Testing facility Dětřichov

The facility is suitable for various pre-clinical experimental studies.

  • Residue depletion studies of products intended for use in food-producing animals
  • Pharmacokinetic studies (bioequivalence)
  • Feed additives studies
  • Clinical trials in cooperation with Czech farms and breeders.

 

Our new modern facility was authorised in 2022. The testing facility 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)

 

Our Dětřichov site serves as the central hub for Tekrolab’s research activities. It is equipped with modern animal facilities designed in accordance with European welfare standards, ensuring safe and ethical conditions for all studies. The site supports pharmacokinetic, bioavailability, bioequivalence, and residue depletion trials in food-producing animals. Our veterinary and technical teams provide expert care, precise data collection, and GLP-compliant study execution. 

 

Analytical laboratory

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

  • HPLC, UPLC-MS/MS, HPLC, LC-MS/MS, method development and validation
  • In-house analytical lab (GLP, GMP compliant)
  • Sample storage and processing under controlled conditions (up to -80 degrees) 
  • Chromatographic, spectral and titration methods (ICH/VICH)
  • Biochemical and hematological analyses (Biochemical, hematological and histological analyses) 
  • Other analyses externally (GC, HRMS, NMR)
  • 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

 

Our laboratory offers advanced analytical services to support veterinary research and development. We specialize in method development, validation, and routine sample analysis for pharmacokinetic and residue depletion studies. Stability programs are conducted under ICH and VICH guidelines, with full GLP compliance. Every step is monitored by our independent Quality Assurance unit, ensuring reliable and audit-ready results. The lab team collaborates closely with study directors and clients to deliver data that meets the highest scientific and regulatory standards. 

Analytical laboratory

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

  • HPLC, UPLC-MS/MS, HPLC, LC-MS/MS, method development and validation
  • In-house analytical lab (GLP, GMP compliant)
  • Sample storage and processing under controlled conditions (up to -80 degrees) 
  • Chromatographic, spectral and titration methods (ICH/VICH)
  • Biochemical and hematological analyses (Biochemical, hematological and histological analyses) 
  • Other analyses externally (GC, HRMS, NMR)
  • 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

 

Our laboratory offers advanced analytical services to support veterinary research and development. We specialize in method development, validation, and routine sample analysis for pharmacokinetic and residue depletion studies. Stability programs are conducted under ICH and VICH guidelines, with full GLP compliance. Every step is monitored by our independent Quality Assurance unit, ensuring reliable and audit-ready results. The lab team collaborates closely with study directors and clients to deliver data that meets the highest scientific and regulatory standards. 

Manufacturing site – GMP production

in your product development and manufacture process – from pre-formulation issues to GMP production of your VMP. Our assistance may comprise: 

  • Ensuring the most stable dosage form 
  • Compatibility of the selected API
  • Stability testing
  • Services of our analytical laboratory
  • VMP release testing by Qualified Person (QP) (to EU from third countries)

 

Tekro has started the production of its own veterinary medicinal products (VMPs). Today, Tekro is one of the most significant producer of VMPs for livestock in the Czech Republic, exporting its production to Central and Eastern European countries. 

We specialize in non-sterile premixes, pulvises, tablets and controlled release forms with following active substances: potassium clavulanate, milbemycin, pleuromutilins, avermectins, amoxicilin, tiamulin, colistin, potentiated sulfonamides and tetracyclines. 

Our manufacturing site provides flexible, GMP-compliant production for veterinary medicines. We support clients from early formulation development through to pilot and commercial-scale batches. 

The facility is designed for small- to medium-scale production, ensuring agility and cost efficiency. Services include formulation optimization, scale-up support, stability testing, packaging, and batch release. With strong QA systems and regulatory compliance, we deliver safe, consistent, and high-quality products to meet both EU and international standards.