Medplum enables building and delivering custom clinical decision support tools for a variety of applications. This guide focuses on the regulated ONC Criteria for Clinical Decision support which is criteria (a)(9) of the HTI criteria on predictive CDS.
Medplum captures consents and signatures as structured, versioned FHIR data rather than as opaque PDFs. The Consent resource is the primitive: it records what a patient agreed to, when they agreed, which policy governed the agreement, and — because every write is versioned — who recorded it and what changed afterward.
Good Manufacturing Practices (GMP) are a set of guidelines, regulations, and quality management systems designed to ensure that products, particularly pharmaceuticals, medical devices, and food products, are consistently manufactured, controlled, and tested according to established quality standards.