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!