Clinical services

Cromos Pharma can manage both single- and multi-center phase I-IV trials in a wide range of therapeutic areas. We also provide services on conduction of bioequivalence studies.

Our project management team is proactive, with effective communication across the spectrum. Responsibilities, processes and reporting lines are clearly defined at an early stage. These procedures are approved step by step to ensure complete transparency.

The primary point of contact will be the Project Manager who will give your study absolute priority, ensuring that timelines are met, quality is maintained, appropriate training is delivered and the budget is adhered to.

Experienced physicians monitor our clinical trials. They are citizens of respective countries, fluent in English and have good knowledge of the local medical community and of therapeutic standards. Our CRAs have undergone extensive training to ensure complete ICH GCP understanding and have industry-related experience of 2-5 years and research experience of at least 2 years.  Their selection is based on both level of experience and professional capabilities.

While working with us you can be sure that CRA assigned to your study will not be replaced by another CRA (except for insurmountable obstacles). It is our policy to keep the same CRA for the lifetime of your study.

We also have a dedicated staff available 24/7 to reply to your requests regarding study and to support investigators.

Our CRAs also can conduct unblinded pharmacy monitoring visits.

If you are interested in clinical research services provided by our company, just This e-mail address is being protected from spambots. You need JavaScript enabled to view it or call Dr. Vladimir Krechikov.