The regulations your
institution must meet today.
What each regulation requires, who it applies to and since when. Explained neutrally, with the official source linked on every page.
Resolutions
in force and in transition.
- Resolution 1888 of 2025Clinical record interoperability stopped being a sector project and became an obligation with a deadline.Read about it
- Resolution 948 of 2026It replaces three resolutions, moves the technical annexes out of the regulatory text and tightens validations. With dates in June, July and September 2026.Read about it
Concepts and processes
every provider needs to master.
- Electronic health record interoperability (IHCE)What IHCE is, which regulations created and regulated it, how clinical data exchange works and what a provider's software needs in order to connect.Read the guide
- RDA, the digital care summaryWhat the RDA is, what types exist, what data it carries, which standard it is built on (HL7 FHIR R4) and how an IPS system generates and sends it.Read the guide
- RIPS in ColombiaWhat RIPS is, how it is generated, how MUV validation works, what the CUV is and what IPS software must do so the invoice is not rejected.Read the guide
- SIIFAWhat SIIFA is, which regulations created it, its four modules, who must report and what an IPS's software must do to integrate with it.Read the guide
Start with a
tailored demo.
Tell us about your institution: size, critical modules and current operation. We set up a demo focused on your case, with no generic presentations or empty promises.
- A demo with your sites, specialties and critical modules
- We get back to you in under 24 business hours
- Pricing per site and active modules, with no per-user licenses
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