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ABOUT US

… You develop the ideas, we can help you navigate through challenges of preclinical research

Mission & vision

We are dedicated to being a reliable partner for our clients in bringing innovative ideas to market, with unwavering adherence to scientific integrity and business ethics.

Our goal is to be recognized as a trusted and respected partner in the field of drug development — known for our strong team of top-tier experts, high professional standards, flexibility, and a personalized, friendly approach to every client.

We strive for excellence in both operations and service by expertise. Through close collaboration with the scientific community, we ensure the highest quality of our services and continually work to enhance client satisfaction.

Expertise & Quality

  • More than 25 years active in human preclinical toxicology
  • Long-term experience in veterinary drug development
  • Extensive experience with variety of compounds and therapeutic areas
  • Expert team capable to conduct studies in full compliance with GLP standards and international guidelines (EMA/ICH, VICH, OECD, US FDA, ISO10993)
  • A pipeline of development of disease models
Compliance with OECD Principles of GLP and OECD, EMA/ICH, VICH, ISO 10993 guidelines
Independent QA conducts regular inspections of the facility, methods, and procedures, as well as reviews of all studies are carried out.
  • Good Laboratory Practice Certificate according to the Principles of OECD C(81)30(Final) issued by State Institute for Drug Control (SÚKL) for pharmaceuticals, medical devices, food additives
  • Good Laboratory Practice Certificate according to the Principles of OECD C(81)30(Final) issued by Ministry of Environment (NIO ASLAB) for chemicals and chemical preparation
  • Authorization for Using of Experimental Animals issued by the Ministry of Agriculture
  • Authorization for Breeding of Experimental Animals issued by the Ministry of Agriculture.

Other Certifications

  • Authorization for restricted handling GMO in compliance with Act No. 78/2004 Collection of Laws.
  • Authorization for handling psychotropic substances issued by Ministry of Health of the Czech Republic according to Gazette Law No. 167/1998 Coll. of Laws.
  • CIR (Credit Impôt Recherche)
Quality
Compliance with OECD TG, EMA/ICH, VICH, ISO 10993
Human health
Compliance with OECD TG, EMA/ICH, EFSA, ISO 10993
Animal health
Compliance with VICH, EFSA
Medical device
Compliance with OECD TG, ISO 10993

Collaborations & References

Collaborations

References

  • Argenta, Germany
  • Artialis, Belgium
  • Asahi KASEI – ViruSure, Austria
  • Biovet AD, Belgium
  • CHR. HANSEN, Denmark
  • Dômes Pharma, France
  • Dicot, Sweden
  • Fatro, Italy
  • Herantis, Finland
  • HUVE Pharma, Belgium
  • Lupin Pharma, India
  • Phileo-Lesaffre, France
  • Polpharma, Poland
  • RCSI, Ireland
  • University Medical Center Groningen,
    The Netherland
  • Virbac, France
  • Vet-Agro, Poland
  • VetBiobank, France
  • Zentiva, Czech Republic

Address

MediTox s.r.o.,
Pod Zámkem 279,
281 25 Konárovice, Czech Republic

E-mail

business@meditox.eu project.manager@meditox.eu

company ID

25926713

vat number

CZ25926713
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MediTox s.r.o.,
Pod Zámkem 279,
281 25 Konárovice, Czech Republic
business@meditox.eu project.manager@meditox.eu
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