Services

What will AGI do for Experimental medicine services?

Positioning for this Coordinate is coming soon.

The work itself

Grounded Work Profile

Tools

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

Outputs

  • Clinical Study ReportserviceBlueprint
  • Adverse Event DatasetserviceBlueprint
  • Biomarker Results DatasetserviceBlueprint

Measured by

  • Protocol Compliance RateserviceBlueprint
  • Adverse Event Reporting TimelinessserviceBlueprint

Key steps

  • Design early-phase study protocolserviceBlueprint
  • Secure ethics and regulatory approvalserviceBlueprint
  • Recruit and consent participantsserviceBlueprint
  • Administer investigational treatmentserviceBlueprint
  • Collect biomarker and safety dataserviceBlueprint
  • Monitor adverse eventsserviceBlueprint
  • Analyze trial endpointsserviceBlueprint
  • Report study findingsserviceBlueprint

How AGI delivers it

Four ways AGI delivers for Experimental medicine services

  • 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 Experimental medicine services connects

absorbs

  • Early Phase Clinical Development Processmodel
  • Early Phase Drug Development Processmodel

composes

measured by

  • Adverse Event Reporting Timelinessmodel
  • Protocol Compliance Ratemodel

optimizes

  • Clinical Data Qualitymodel
  • Data Query Resolution Timemodel
  • Participant Safetymodel
  • Patient Recruitment Ratemodel

produces

  • Adverse Event Datasetmodel
  • Adverse Event Logmodel
  • Biomarker Results Datasetmodel
  • Clinical Study Reportmodel
  • Pharmacokinetic Datasetmodel

realizes

  • Administer investigational dosemodel
  • Administer investigational treatmentmodel
  • Analyze trial endpointsmodel
  • Collect biomarker and safety datamodel
  • Collect pharmacokinetic samplesmodel
  • Deliver clinical study reportmodel
  • Design early-phase study protocolmodel
  • Monitor adverse eventsmodel
  • Monitor and report adverse eventsmodel
  • Obtain ethics and regulatory approvalmodel
  • Recruit and consent participantsmodel
  • Report study findingsmodel
  • Scope study protocol with sponsormodel
  • Secure ethics and regulatory approvalmodel