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Clinical trial specialists of Vita Aeterna company provide the full range of services on checking of subject safety, compliance with the protocol, GCP, national legislation and quality of data collection.


  • Making qualification visits, initiation visits, routine monitoring visits, site closure visits;

  • Effective interaction with study sites;

  • Making investigator trainings;

  • Checking patient informed consents;

  • Checking patient compliance with the protocol criteria;

  • Checking the Investigator file for provision of adequate maintenance and document storage;

  • Checking study sites data including source documents and completed CRFs;

  • Collection of study documents including regulatory documents;

  • Accountability of a study drug and comparator;

  • Tracking patient enrollment status in each site;

  • Checking SAE reports;

  • QUERY management;