• 1
  • 2
  • 3

    Ascent CRS is a full-service CRO that provides an entire range of clinical research services from Phase I and Proof of Concept to Phase III-IV and Bioequivalence studies.

  • 4
  • 5
  • 7
  • 9

Phase III-IV studies

These clinical trials are the large scale testing, which would involve several hundred to several thousand patients and could last for several years, which requires excellent understanding and managing at a global scale.

Although we specialize in early development phases, we have en extensive track record of advancing new drugs through late phase clinical trials. These have ranged from small, single country marketing studies through to large global observational trials.

Strong connections with sites and investigators, own base of freelance monitors covering all of the territory of Russia and Georgia, excellent regulatory knowledge, own electronic system for managing clinical trials will help you conduct pivotal trials faster while minimizing risks, costs and delays.

Ascent CRS not only provides a complete range of clinical study services for the Phase III to Phase IV  studies.

We also create and manage the following:

✓ Safety surveillance studies
✓ Large simple studies
✓ Retrospective and prospective chart reviews (single-site or multi-centre)
✓ Health outcomes research
✓ Patient-reported outcomes
✓ Site management (remote and on-site)
✓ Subject recruitment and retention plans

Experienced clinical operations team provides strong site management and enrollment strategies while our medical monitors provide vital oversight with a strong focus on safety.

Covering territory with 150 million of people we have developed strong network of large-scale, country-wise sites and investigators in mostly all therapeutic areas.

Our experts can help you navigate through all available design/management options, avoid study over-engineering, and ensure that you meet your clinical objectives within budget.

We offer following services:

▪ Medical writing
▪ Site and investigator selection
▪ Project Management
▪ CRA activities/monitoring
▪ Regulatory support, incl. import & export of medication
▪ Data Management and Statistics

Services can be contracted either as a comprehensive package to manage your entire study, or on a selective basis when additional resources and services are required.

We have conducted multiple trials internationally, tapping into our network of global CRO partners as needed.

With our full range of services, you gain end-to-end planning to build quality into your trials from the start, to mitigate risk, gain cost and time efficiencies, and optimize performance to meet critical milestones.

We’re dedicated to the success of your study!