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Health Care Institution
  • Access to the latest treatment possibilities and approaches to tackle diseases
  • Possibility to help patients
  • Participation in international projects
  • No concerns regarding management and organization of clinical trials
CRO
  • Feasibility questionnaires are completed by Principal Investigators in the least amount of time due of the provided assistance
  • Referral of prospect patients to the research sites to meet the objectives of the clinical trials
  • Assistance during the preparation and enrolment periods to include maximum number potential patients during the minimum amount of time
  • Preparation and training of new investigators
  • Sites quality assurance in accordance with Good Clinical Practice
  • Assurance that the process of clinical trials is arranged in accordance with the international regulations, requirements of Good Clinical Practice, local legislation and special requirements
  • Quality check of clinical trial related documentation (eCRF, temperature logs, subject logs, study drug accountability logs, etc.)
  • Assistance in solving complicated and additional questions from investigators
  • Contact with medical institutions to ensure faster and efficient management of clinical research as well as execution of legal and financial contracts
Sponsors
  • Increase number of patients and research centers
  • Guaranteed high quality conduct of clinical trial
  • Ensure meeting timelines through all study stages
  • Evaluation and selection of potential centers for clinical trials
  • Professional partner for everyday contacts