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A better way for Sponsors/CROs and Research Sites to connect

For Research Sites

Ravek identifies new study opportunities for your research site. We qualify your teamwork and support all project needs and respective tasks. All these benefits are matched with our experience and expertise in clinical research service.

For Sponsors and CROs

Ravek provides sponsors and CROs access to potential investigators, best qualified research sites and target study population. All these benefits are matched with our experience and expertise in clinical research service.

> Let's make life better...

Excellence in Clinical Research Service

For Sponsor and CROs
Competitive Benefits
  • Find experience and expertise working hand in hand to support your clinical trial.
  • Rapid access to the target research site and respective target population.
  • One contract and one budget for all sites selected on the trial.
  • Individually assigned accounting manager to handle all site payments.
  • Single point of contact for feasibility and contract/budget negotiations.
  • Assistance with site management, communications and study updates.

  • Last, but not least, save billable hours in your budget. 

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Operational Services:
  • Feasibility
  • Study Start up
  • Regulatory Affairs Submissions
  • Contract Preparation
  • Prospect Target Population
  • Patient Recruitment & Retention
  • Support Study Visits (Initiation, Monitoring and Close out)
  • Filling CRFs and Study Forms
  • AE and SAE Report
  • Study Drug Management & Accountability
  • Site Project Management
  • Site Training
For Research Sites
Competitive Benefits
  • Find experience and expertise working hand in hand to support your clinical trial.
  • Access to hundred of new clinical trials each year.
  • Access to new sponsors and CROs.
  • Accelerate your study start-up process
  • Get rapid access to the target  population.
  • Get better study trial management in your site.
  • Get assigned accounting manager to handle all site payments and control the budget
  • Assistance with sponsor/CROs communications and study updates.
  • Last, but not least, get better solutions to manage trial business in your research site.
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Operational Services:
  • Feasibility
  • Study Start up
  • Regulatory Affairs Submissions
  • Contract Liasion
  • Patient Recruitment & Retention
  • Support Study Visits ( Initiation, Monitoring and Close out)
  • Filling CRFs and Study Forms
  • AE and SAE Report
  • Study Drug Management & Accountability
  • Site Project Management
  • Payment and Budget Control
  • Site Training

  • Quality Assurance / Mock Audits

 
Business Services:
  • Prospection of New Study Opportunities

Experience and Expertise go hand in hand

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