Sponsors & CROs

 

Sponsor care about time dedicated to the clinical research that is why we are accelerating drugs and medical device development. We minimize the time required to complete clinical research and get qualifying drugs and devices to market.

We simplify the process for sponsors and CROs by providing access to member sites meeting the highest standards of quality and productivity.

The network includes member sites:

  • Located in Poland

  • Phase I, II, III, & IV studies

  • Inpatient & Outpatient studies

  • Each site is independently owned and operated

  • Central IRBs/IECs acceptable (or local Accredited IRBs/IECs guarantee quick turnaround of submissions)

  • Accepted through a rigorous qualification process ensuring high rates of:

    • Enrollment

    • Retention

    • Completion

    • Evaluable data rates

    • Quick query solving

    • Data Entry support

  •  Low Rates of Queries per CRF (on average compared to other sites conducting the same study on prior studies conducted)
     

Sponsors and CROs achieve efficiencies and cost savings resulting:

  • Sites pre-qualified for individual trials based on past performance on similar studies

  • Recruitment capabilities relative to study specific requirements and inclusion/exclusion criteria

  • Access to different patients populations

  • Centralized budget and CTA negotiation and administration

  • Prompt turnaround time of regulatory documents

  • Increased productivity and quality of network members via proprietary processes to share best practices in GCP, recruitment, and retention
     

Sites are strategically located to maximize enrollment potential and minimize sponsor and CRO travel time and costs.

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