Global Research Partner LLC

Global Research Partner (GRP) is a premier organization in Ukraine, offering a full spectrum of services for the management and execution of clinical trials. As both a Contract Research Organization (CRO) and a Site Management Organization (SMO), we ensure that research sites operate at the highest international standards while helping sponsors bring groundbreaking treatments to market efficiently and ethically.

Committed to excellence, innovation, and compliance, GRP stands at the forefront of clinical research in Ukraine, maintaining the same high level of quality, precision, and reliability as the world’s leading CROs. Our expertise spans regulatory support, patient recruitment, site management, and full-cycle clinical trial coordination, ensuring streamlined and successful research processes.

With a deep understanding of the regional healthcare landscape and a strong network of trusted medical institutions and laboratories, we provide tailored solutions that optimize study timelines, enhance data integrity, and accelerate drug development.

At GRP, we don’t just follow global standards—we set them, making us the preferred partner for clinical research in Ukraine and beyond.

Core Principles of Our CRO:

Compliance with International Standards: We strictly adhere to GCP (Good Clinical Practice), ICH (International Council for Harmonisation), and both local and international regulatory requirements.
✓ Ethics and Patient Safety: All studies are conducted with the utmost respect for patient rights and in full compliance with the principles of the Declaration of Helsinki.
✓ Data Quality and Integrity: We ensure accuracy and reliability at every stage of clinical trials.
✓ Transparency and Reproducibility: All processes are well-documented and subject to audits, guaranteeing research reliability.
✓ Innovation and Advanced Technologies: We implement modern tools for data collection and analysis, including digital solutions and automation.
✓ Effective Study Management: Risk minimization, process optimization, and reduction of clinical trial timelines.
✓ Regulatory Compliance and Reliability: We collaborate exclusively with certified laboratories and research centers to ensure the highest level of result reliability.

Additionally, we comply with GDPR (for data protection) and FDA 21 CFR Part 11 (for electronic documentation) and adhere to other industry-relevant regulations.

Services

At GRP, we offer a comprehensive suite of services to support and streamline your clinical research needs:

Before Clinical Trial:

During Clinical Trial:

• Start-Up activities

• LEC documents preparation and submission.

• Budgets discussion/Contracts Negotiations.

• Documents preparation (for ex. CVs, FDA forms, etc.)

• Subject recruitment activities (pre-screening work, maintenance subjects' database, working with referrals and partner sites)

• Feasibility Check-Up

• Site file management.

• Direct cooperation with PM/Monitor or Sponsor representative.

• Providing all requested documentation.

• LEC correspondence.

• Providing all necessary scans and copies during all trial.

• Сontrol over all calibration certificates.

• Control over all-patients visits time frames.

• Control over all Investigators certificates and main documents (periodic updating of documents and updating of data)

• e-CRF completion/ Queries resolving.

• Project-specific trainings.

• Source document work sheets preparation

• Site preparation for audits/ inspections.

After Clinical Trial:

• Final check-up of protocol documentation before archiving.

Additional Services:

• Additional recruiting activities

• Patient transportation services

• Patient Home IP-Delivery

• Patients payments (1phase only)

Get in touch

We are always happy to assist and answer your questions. Please fill out the form below or use our contact details to get in touch.