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A Full-Service Medical Device CRO

JERELO is highly aligned with medical devices!

 We can offer you a business partnership and guidance through your journey involving clinical research projects following the ISO 9001 certified quality system. We ensure good clinical results, adherence to budget and schedule, improvement of data integration and contract management.

We are eligible to assist you with research projects further, including but not limited to the following: Early Feasibility, First-in-Man, and Multicenter Prospective Observational studies.

Since every project is unique, the needs and regulatory requirements vary from project to project. Hence, our multidisciplinary team can help you with various types of studies and make sure that your clinical research project is completed in the most optimal way possible.

Our services include but are not limited to, the following:

  • Protocol Design and Development
  • Investigator’s Brochure Writing
  • Development of Instructions for Use
  • Designing Case Report Form
  • Informed Consent Guidance
  • Party Selection
  • Investigator Selection
  • Management of Clinical Trial Agreements
  • Regulatory and Ethics Committee Submissions
  • Clinical Project Management
  • Clinical Evaluation Report Writing
  • Product Training
  • Party Monitoring
  • Clinical Research Coordination
  • Safety Reporting
  • Data Management and Statistics
  • Clinical Auditing

As a full-service CRO, JERELO can satisfy your needs and requirements at any stage of your clinical research project!

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CONTACT Us

33B, Shota Rustaveli str., Kyiv, 01033, Ukraine

+380 (95) 692 26 08

daria.abulova@jerelo.eu

Mon - Sat | 9am - 8pm

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