Atlant Clinical CRO - clinical trials in USA, Russia and Europe

Welcome to Atlant Clinical, a reliable and efficient provider of clinical research services in the USA, Europe, Russia, Middle Asia, and Baltic States. Our team employs about 150 professionals in clinical research working worldwide. Approximately 90% of our employees have scientific background, 30% are M.D.s, and 10% have Ph.D.s. We closely work with sponsors providing them with tailored and efficient solutions for every project. As a result, we take great pride in creating lasting and gratifying relationships with our clients worldwide. Our philosophy is focused on our clients, and it makes our contract research organization a preferred supplier for such leading companies as GSK and MSD. It is based on the following principles and values:

Transparency
Quality
Integrity
Speed
Value

Full Range of Clinical Trial and Support Services

Established in 2007, our international CRO offers extensive experience and expertise
in Phase I–IV clinical trials and a vast number of support services.

Medical and Scientific Advising

  • Translation and adaptation of trial documentation
  • Scientific and medical project assessment
  • Preparation of clinical study report
  • Preparation of medical and scientific articles for international and local peer-review journals
  • Development of patient-doctor diaries and questionnaires

Services in Clinical Operations

  • Project management
  • Study start-up
  • Clinical monitoring
  • Site management
  • Safety monitoring
  • Logistics management services
  • Vendors’ management

Regulatory Support

  • Trial dossier preparation and submission to regulatory authorities
  • Obtainment of import/export licenses for drug(s) and other supplies in clinical trials
  • Timely submission of safety reporting in accordance with local regulations and ICH GCP
  • Timely submission of required documents to ethics committees and/or regulatory authorities

Data Management

  • Data management plan preparation
  • Electronic data capture system creation, user support, and ongoing entered
    data quality monitoring and verification
  • Development of electronic and paper CRFs

Biostatistics services

  • Statistical analysis plan creation
  • Statistical data analysis
  • Statistical programming (SPSS, SAS and others)
  • Drug labeling list preparation
  • Interim and final statistical reports writing

Quality assurance

  • Certified audits of investigational sites, vendors, phase I units, SOPs, and TMFs
  • QA consulting