Clinical Accelerator maintains a network of over 100 affiliate investigative sites in our CEE region of operation (ClinAccel.Net)

We conduct our own clinical studies through ClinAccel.Net, and connect members of the network with other clinical CROs and sponsors.

Our model of work is centered on the imperative to accelerate the implementation of clinical trials. We always try to use a minimal number of highly efficient sites to achieve our patient enrolment targets.

ClinAccel.Net includes primary, secondary and tertiary care healthcare institutions, in-patient and out-patient facilities, generalist and specialist sites working in all major therapeutic areas.

As our model work is centered on the ability to accelerate implementation of clinical trials, Clinical Accelerator provides the following important services to members of ClinAccel.Net:

  • Site training
    • GCP training programs
    • Site SOP development and implementation
    • Investigator meetings
  • Acceleration of clinical start-up cycle
    • Expedited site selection
    • Study budgeting
    • Study contracting (one central contract for members of ClinAccel.Net participating in one study)
    • Site documentation required for local clinical trial authorizations
    • Local Competent Authority and Ethics Committee (IRB) approvals
    • Study logistics, site and vendor payments
  • Acceleration of patient identification and enrolment
    • Evidence-based feasibility
    • Identification of qualified patients
    • Patient enrolment planning
    • Patient enrolment and retention strategies
  • Patient retention
    • Patient retention strategies
  • Additional site resources for efficient study implementation
    • Study coordinators
  • Advisory services
    • Scientific Advisory Board consists of local key opinion leaders (K.O.L.s) representing members of CliniAccel.Net