AGI.do

Services

What will AGI do for Clinical human drug trials?

In this classification, this commodity consists of comprehensive services required to be a clinical human drug trial service

The work itself

Grounded Work Profile

Tools

  • Clinical Trial Management SystemserviceBlueprint
  • Regulatory Submission SoftwareserviceBlueprint
  • Patient Recruitment PlatformserviceBlueprint
  • Electronic Data Capture SystemserviceBlueprint
  • Pharmacovigilance SystemserviceBlueprint
  • Statistical Analysis SoftwareserviceBlueprint

Outputs

  • Trial Participant RecordsserviceBlueprint
  • Adverse Event ReportsserviceBlueprint
  • Clinical Study ReportsserviceBlueprint

Measured by

  • Data Accuracy RateserviceBlueprint
  • Adverse Event Reporting TimelinessserviceBlueprint

Key steps

  • Design Trial ProtocolserviceBlueprint
  • Obtain Ethics Board ApprovalserviceBlueprint
  • Recruit And Consent ParticipantsserviceBlueprint
  • Administer Study DrugserviceBlueprint
  • Monitor Adverse EventsserviceBlueprint
  • Analyze Trial DataserviceBlueprint
  • Submit Clinical Study ReportserviceBlueprint

How AGI delivers it

Four ways AGI delivers for Clinical human drug trials

  • Services-as-Software

    Get the professional outcome delivered as software, priced on results, not headcount.

    Services.do

  • Autonomous Agents as digital employees

    Hire a digital employee that does the job under earned, supervised autonomy.

    Agents.do

Value flow

How Clinical human drug trials connects

absorbs

  • Clinical Developmentmodel
  • Clinical Trial Monitoring Processmodel
  • Drug Safety Monitoringmodel

composes

measured by

  • Adverse Event Reporting Timelinessmodel
  • Data Accuracy Ratemodel
  • Data Integrity Scoremodel
  • Protocol Compliance Ratemodel

optimizes

  • Data Query Resolution Timemodel
  • Patient Enrollment Ratemodel
  • Protocol Adherencemodel

produces

  • Adverse Event Datasetmodel
  • Adverse Event Reportsmodel
  • Clinical Study Reportmodel
  • Clinical Study Reportsmodel
  • Patient Outcome Recordsmodel
  • Trial Participant Recordsmodel

realizes

  • Administer Study Drugmodel
  • Administer investigational treatmentmodel
  • Analyze Trial Datamodel
  • Analyze trial outcome datamodel
  • Define trial protocol with sponsormodel
  • Deliver clinical study reportmodel
  • Design Trial Protocolmodel
  • Monitor Adverse Eventsmodel
  • Monitor adverse eventsmodel
  • Obtain Ethics Board Approvalmodel
  • Obtain ethics board approvalmodel
  • Recruit And Consent Participantsmodel
  • Recruit and consent participantsmodel
  • Submit Clinical Study Reportmodel

Go deeper

Explore Clinical human drug trials

Read the deeper take on agi.asView as markdown