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Test participant clinical trial procedure guidelines

Steps Contents
Establish schedule Studies that require clinical trials
Clinical trial planning phase
Clinical trial inquiry Scope and methodology of clinical trials
Inquiries regarding expenses
Planning development Develop a plan to test the function being studied by the researcher
Research plan contract engagement Phase in which contract is reviewed and finalized
Clinical trial schedule Phase in which researchers’ requests are applied to clinical trial plans
and contractual requirements are finalized
Contract Phase in which clinical trial center and
clinical trial contracts are signed
Provide test sample Phase in which test materials are provided to research center
in accordance with contractual obligations
Clinical trial monitoring Phase in which clinical trials are conducted
and monitored in accordance with contractual obligations
Receive clinical trial result reports Phase in which clinical trial result reports are received
in accordance with contractual obligations
Clinical trial completion Phase in which clinical trial studies are completed and terminated

Center receive clinical trial procedure guidelines

Phase Contents
Test plan review and consultation Cost disclosures based
on clinical trial scope, plans,
procedures, and scale
Develop plans and contracts Phase in which researcher discloses goals,
methods and advises on the clinical aspect of the study
Contract Phase in which test participants engage in contracts to join clinical trials
Recruiting and screening test participants Phase in which test participants are recruited
and selected test participants for research are announced
Receive test samples Verification of test substances and researcher receives materials
in accordance with contractual obligations
Conduct clinical trials Phase in which clinical trials are conducted in
accordance with contractual obligations
Submission of clinical trial result reports Phase in which client receives clinical trial result information
in accordance with contractual obligations
(All data related to tests shall be provided upon request)
Internal quality-control management Phase in which all clinical trial contents are reviewed to ensure
and improve quality levels and controls
Clinical trial completion Phase in which clinical trials are completed