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Clinical Trial Services

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ClinTrial provides a comprehensive portfolio of services covering all phases of clinical research. ClinTrial conducts all clinical monitoring and related activities under GCP standards and in accordance with applicable law.


Clinical studies

Phase I-IV domestic and multinational trials

  • Study design, protocol development, case report form design and printing
  • Site and investigator selection and recruitment
  • Regulatory and ethical approval procurement, preparation and review of regulatory submissions, interaction with regulatory agency
  • Continuous liaison with investigators
  • Management of patient recruitment
  • Site management and monitoring based on Standard Operating Procedures and study-specific check-lists (site initiation, regular monitoring visits, source data verification, monitoring visit reports, adverse event reports, site closure visits)
  • Data management services and trial administration (validated data entry, database design, data upload, computerised error detection and data checking, data queries, filing system design and implementation)
  • Electronic information systems (investigator’s information, data handling guidelines, online status reports)
  • Statistical evaluation
  • Interim status report, final report and media presentation

 

Clinical pharmacological investigation site

 

Clinical testing of medical equipment

  • Prosthetic devices
  • Vessel grafts
  • Machinery and equipment
  • Bandages
  • Blood sampling tools, needles, syringes
  • Implants
  • Plastic surgery applications

 

Pharmacovigilance

  • Design, implementation and maintenance of drug safety reporting systems
  • GCP compliance monitoring of all aspects related to trial drug
   
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