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Tekrolab

Your partner in Preclinical Research

and Pharmaceutical Industry

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Tekrolab

Your partner in Pharmaceutical industry and Animal health
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Contract Research

  • Preclinical studies for human and veterinary pharma R&D 
  • Pharmacokinetic studies, residue depletion studies, feed trials 
  • Own GLP certified testing facility and analytical laboratory 
  • Accredited to use animal models (pigs, cattle, sheep, poultry)
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Contract Manufacturing

  • Solid dosage forms (premixes, pelvises, tablets) 
  • GMP certified 
  • Various active substances (penicilines, tetracyclines, potentiated sulphonamides) 
  • Stability testing 
  • VMP release testing by QP based in EU 
  • Cooperation with scientific institutions 
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Pharmacovigilance

  • Complete outsourcing of pharmacovigilance system for MAH 
  • PSMF preparation 
  • Benefit-risk balance assessment 
  • Services of QPPV based in EU 
  • Consultations and training in pharmacovigilance 
  • Scientific literature reviews
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News

Successful Webinar Brought Together Professionals from Across the EU

4. 2. 2026

On 28 January, Tekrolab hosted an online webinar “Basics of Veterinary Pharmacovigilance”, bringing together professionals from across the European Union working in veterinary pharmaceuticals, regulatory affairs, and pharmacovigilance. The webinar focused on the core principles of veterinary pharmacovigilance under Regulation (EU) 2019/6, including system setup, legislation and documentation, adverse event

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From preclinical trials and lab analyses to pharmacovigilance and regulatory approval — we deliver end-to-end services under one roof. 

  • Over 30 years of experience in pharma industry, animal health and contract research 
  • Certified labs, GMP & GLP infrastructure, own farms and animals 
  • Integrated services: research, development, manufacturing, PV & RA 
  • Focus on quality, animal welfare, and regulatory compliance 
  • Our offer – flexible, secure and reliable partnership. 
Who we are?
  • Tekrolab is veterinary CRO & CDMO of Tekro Ltd from Czech Republic. We offer a complex range of services in Animal Health and Veterinary industry – from development and manufacturing of veterinary medicinal products, through their testing, to post marketing surveillance.
  • We are here for all Marketing Authorisation Holders (MAH) of veterinary medicines and other entities (CRO, CMO, R&D labs or regulatory companies) in veterinary area. We can find right solution for worldwide corporates or for regional companies.

What we do?

  • CRO: We conduct commercial pre-clinical studies mainly in livestock in our own GLP certified testing facility in Dětřichov (Czech Republic). We also offer analytical services of our well-equipped laboratory.
  • CDMO: We produce veterinary medicinal products and feed additives for livestock in manufacturing plant Nová Dědina (Czech Republic). We specialize in premixes, pulvises and tablets (ivermectin, amoxicillin, tiamulin, colistin, potentiated sulphonamides and tetracyclines). We also offer Veterinary pharmacovigilance outsourcing.

Our vision

  • Our vision is to support your veterinary medicinal product throughout the development life cycle towards the marketing authorization and maintenance. We achieve this by implementing sound business strategies, fostering proactive and committed teams, adhering to globally accepted standards and protocols, prioritizing customer satisfaction, and ensuring the welfare of animals in every aspect of our operations.

How we work?

  • Our services are based on our own experience gained during the development, testing and production of our proprietary veterinary medicines. Because of this, we know what we are doing. By learning from our own mistakes we gurantee complex and individual approach to every client. With us, you don’t have to start from scratch. You will be one step ahead.

Registration Form

Basics of Veterinary Pharmacovigilance

We will send you the proforma invoice within 24 hours.

January 28, 2026 | 9:00-15:00 | Online