Our Members

We are proud to house a family of innovative members.


    LAUS GmbH
    Germany


    LAUS GmbH is a family owned, independent contract research organization (CRO) specializing in GLP-compliant       studies for regulatory and compliance purposes. Founded in 1991 and GLP-certified since 1999, LAUS has more than       three  decades of experience supporting customers from the chemical, pharmaceutical and biocide industries.

                                                                                         Our laboratory is certified for the GLP test facility categories 1 (Physico-chemical Testing), 3 (In Vitro Toxicology) incl.                                                                                            genotoxicity, 4 (Ecotoxicology), 5 (Environmental Fate), 6 (Residue Studies) and 8 (Analytical and Bioanalytical Studies).

                                                                                         We provide high-quality experimental data to support regulatory compliance under international guidelines and                                                                                                    legislation. Our expertise includes studies for chemicals under REACH, including nanomaterials and polymers,                                                                                            biocidal active substances and products under the Biocidal Product Regulation, and Environmental Risk                                                                                            Assessments (ERA) and in vitro genotoxicity testing for human medicinal products in accordance with EMA                                                                                            requirements.

                                                                                         Committed to scientific excellence, quality and regulatory compliance, LAUS is a trusted partner for companies                                                                                            requiring reliable data for product registration and market approval worldwide.


Institute of Experimental Pharmacology and Toxicology / Centre of Experimental Medicine of the Slovak Academy of Sciences 
Slovakia

The Centre of Experimental Medicine (CEM) of the Slovak Academy of Sciences (SAS) was established by merging of the Institute of Experimental Pharmacology and Toxicology, the Institute of Normal and Pathological Physiology and the Institute of Heart Research into one Centre. CEM is focused on the integrated research into the causes, mechanisms of development and possibilities of prevention, diagnosis and treatment of societally important diseases with the emphasis on diseases of the cardiovascular and the nervous systems, metabolic disorders, mental disorders and mental health problems as well as diseases originating in the prenatal and early postnatal developmental periods. The research in CEM is carried out on in silico, in vitro, ex vivoain vivo models with the aim to transfer the acquired knowledge to clinical practice.

 

An important part is the evaluation of the effects of bioactive natural substances, their derivatives and original synthetic substances with pharmacotherapeutic potential, on animal models of human diseases and human samples, as well as the study of side effects and toxic effects of chemicals and radiation.

 

The facilty has been GLP recertified in 2019 ad has an expertise for many regulatory in vivo acute, semichronic and chronic toxicological and safety studies with a special part to reproductive & development studies on rats and rabbits. The GLP certifctaion also includes a state-of-the art in vitro toxiclogy lab for determination of adverse effects of test items to skin, eye and other tissues in vitro.


Cluster PharmValley
Russia


The cluster PharmValley associates a wide spectrum of Russian research and science institutions to conduct a complex portfolio of services incl. development, GLP preclinical, clinical, toxicity and safety studies, preparation of registration dossier and registration, synthesis of pharmaceutical substances, development of finished dosage form and other services necessary for the creation of drugs and medical products. The key cluster specialization are pharmaceuticals, notwithstanding the other core business are apparent as well:
  • Medical industry incl. medical devices
  • Chemical substances and preparations
  • New materials
  • Industrial biotechnologies (manufacture of products based on enzymes and microorganisms to be used further in chemical industry, healthcare, manufacture of food products and feeds, washing agents, paper and cellulose, textiles, as well bioenergetics)

 

The PharmValley represents full-cycle activities (development, preclinical and clinical studies, preparation of a registration dossier and registration, synthesis of pharmaceutical substances, development of a finished dosage form) and services necessary for manufacture of drugs and medical devices for pharmaceutical industry in accordance with international standards of the good practices (GLP, GCP and GMP). A special part represents research and studies on primates, at the unique center primatology center in Russia, which is one of the largest in Europe. Preclinical toxicological and safety studies of biomedical drugs, chemical substances and preparations (REACH) and other products on SPF laboratory animals (mice, rats, hamsters), incl. investigation of their pharmacological action and effects are fully performed in compliance with the international GLP standards.


Slovak Medical University
Slovakia


The Slovak Medical University in Bratislava is an educational institution proudly keeping the tradition of education of healthcare workers in specialized studies and continuous life-long education in Slovakia. In 1995, the test facility obtained GLP certificate by Slovak National Accreditation Service and it has It has authorization to use laboratory animals in toxicological and preclinical experiments and studies certified by State Veterinary and Food Administration of the Slovak Republic. The GLP facility is able to perform studies of toxicity, mutagenicity, teratogenicity and reproduction, tests of skin sensibilisation and immunotoxicology studies in specific pathogen free (SPF) Unit.

University Of Veterinary Medicine And Pharmacy
Slovakia


The University of Veterinary Medicine and Pharmacy in Košice (UVMP in Košice), established as the Veterinary College in Košice, is the only institution providing undergraduate, graduate and postgraduate veterinary education and since 2006 also pharmaceutical education in the Slovak Republic.

In addition to huge educational importance, a special member of our cluster represents Department of Pathological Anatomy and Pathological Physiology within the University like a GLP facility specialized for histopathology studies and supporting toxicity studies requiring histopathological assessment of tissues and organs of animal origin.

Comenius University, Jessenius Medical Faculty in Martin (Biomedical Center Martin / BIOMED)
Slovakia


Biomedical Center Martin belongs to the most extensive projects of the Jessenius Faculty of Medicine in Martin of Comenius University in Bratislava.

The workplace is a representative example of efficient use of financial resources and interconnection between research and practice, and represents intellectually stimulating modern space with new approaches, technological procedures, methodologies and unique equipment of laboratories.

The main areas of the expertise are: Molecular medicine, Neurosciences, Oncology and Respirology.

The facility is in the phase of GLP certification, which is going to be completed in 2020 and then facility will be mainly focused on GLP inhalation studies.


SITNO PHARMA, Ltd.
Slovakia


SITNO PHARMA, Ltd. is a member of the Holding Group called Sitno Holding a.s., group of the companies offering Investment Consulting Services, Searching for strategic partners for investment-intensive projects and Crisis Management.

 

                                                                                      Its aim is to integrate and to offer to clients the R&D and pharmaceutical production capacities of our partners in                                                                                         effective scientific cooperation in the fields of chemical sciences, bioinformatics and chemical engineering, industrial                                                                                         biotechnology, pharmaceutical chemistry, pharmacology and toxicology. 
                                                                             
                                                                                      SITNO PHARMA, Ltd. also operates as the main contact, communication, coordination and business point in the                                                                                         InterBioTox cluster. It mutually improves and connects cooperation between cluster members and end customers,                                                                                         strengthens business relationships and increases coherence and competitiveness for the effective operation of                                                                                         members within or outside the cluster. SITNO PHARMA, Ltd. manages all the approved projects from “one hand” for all                                                                                         of our clients.

hameln rds a.s.
Slovakia


hameln rds is a well-recognised pharmaceutical service provider for health-care industry. We focus on different steps during development and production of pharmaceutical products. We are covering analytical and galenical development of pharmaceuticals, Quality Control Services (stabilities and batch release) and development and GMP manufacturing of APIs.

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