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Clinical studies

  • Counsel on clinical studies procedures and on selection of contractors and researchers;
  • Preparation, analysis and editing of contracts necessary for the conduct of clinical studies;
  • Support in negotiations with the relevant state authorities, expert institutions, and medical institutions;
  • Counsel on the protection of personal data during clinical trials and patients' rights.

  • Assessment of compliance of medical devices and equipment with requirements of technical regulations

  • Services for medical institutions

  • Public procurement of medicines and medical devices

  • Confirmation of compliance with the GMP requirements

  • Import and export of medicines and medical devices

  • Medicine advertising

  • Declaration of wholesale and selling prices

  • Registration of drugs

  • Licensing of manufacturers and distributors of medicines

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