Services

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

Before 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

During Clinical Trial

• 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)