Since 2009 ARS PharmRussia has supported Russian and foreign pharmaceuticals and biotechnologies companies in the sphere of drug registration, including required preclinical and clinical studies as well as providing with other consulting services on regulatory and intellectual issues in the pharmaceutical field.

ARS organizes and conducts clinical trials within international clinical programs as well.

In our work we adhere to ICH-GCP, FDA, EMA, EEU and local standards. At the same time ARS helps clients to find more cost-effective ways for drug registration.

The most important measures at our daily work are the following:

  patients’ safety and risk-benefit ratio

  data and processes’ quality

  privacy and confidentiality

  timelines agreed upon by the sponsors

  relationships with investigators

  advanced trainings of the team

  vendors’ qualification

  innovative technologies

  effective clinical project budgeting

  risk management

  professional communication at all levels

We will be glad to meet new people and to find new partnerships!


Russia, Moscow.

Multifanctional complex «Federation»
Presnenskaya embankment, 12
East Tower, 27th floor, 17 room.

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