Clinical Trials Management
Planning, execution, monitoring of clinical studies.
Clinical Trials Management (BC-1520) is a level-1 business capability in the Pharmaceuticals & Life Sciences model. The catalog holds 13 API surface(s) from 6 provider(s) that can perform some part of it. Reach is the vendor surface that lands on this capability — it is not a claim about what any particular organisation has deployed.
Sub-capabilities
Clinical Trial Design Management BC-1520.10
Protocol design, statistical methodology, endpoints.
Clinical Trial Site Management BC-1520.20
Site selection, activation, oversight.
Clinical Trial Subject Management BC-1520.30
Recruitment, screening, retention, informed consent.
Clinical Data Management BC-1520.40
EDC, data capture, query management, database lock.
Clinical Trial Monitoring Management BC-1520.50
Site monitoring, risk-based monitoring, audits.
Clinical Trial Supply Management BC-1520.60
IMP supply, distribution, randomisation, drug accountability.
Clinical Outsourcing & CRO Management BC-1520.70
CRO selection, contracting, oversight.
Providers that reach this capability
Ordered by rating band. Reach means a provider publishes an API surface that can perform some part of this capability — it is not a claim that any particular organisation has deployed it.