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
effective clinical project budgeting
professional communication at all levels
We will be glad to meet new people and to find new partnerships!
contact us by email,
or fill out the request form.
© ARS PHARMRUSSIA: CLINICAL & REGULATORY EXPERT CRO, 2009-2020
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