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 in a step-wise manner to ensure complete transparency.
With every study that we conduct, we appoint a Project Manager with experience in the field of research who acts as a primary liaison for the sponsor and gives your study absolute priority, ensuring that timelines are met, quality is maintained, appropriate training is delivered and the budget is adhered to.
We employ only experienced physicians to monitor our clinical trials. They are citizens of respective countries, fluent in English and have good knowledge of the local medical community and its medical practices and standards. Our CRAs have undergone extensive training to ensure complete ICH GCP understanding and have industry-related experience of 5 years and research experience of at least 3 years.
While working with us you can be assured that the lead 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 dedicated staff available 24/7 to reply to your study inquiries and to support the investigators.
Our CRAs also can conduct unblinded pharmacy monitoring visits.