Drawing upon our 30 years of expertise,
we are honored to facilitate the seamless
execution of your clinical trials

  • Product development studies

  • Selection and supply of reference products and/or test products

  • Generation of study protocols and documentation for Bioethics

  • Pharmacovigilance and safety monitoring service

  • Post-authorization safety studies

  • Import/export and supply of Investigational Medicinal Products (IMP) and Medicines for Clinical trials from non-EU countries

Fill out the inquiry form and receive a consultation, pricing, and a complimentary presentation of our services. Explore collaboration oppurtunities:

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