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Capsule diagnostics platform

The platform behind capsule diagnostics.

Software, AI and logistics that let practices, imaging centers and health systems offer capsule diagnostics in their clinic or in the patient's home.

Capsule endoscope with visible optical camera
12,000+capsule procedures supported since 2015
9operating geographies
82%less colon reading time with AiSPEED™*
6capsule platforms, one workflow
The platform in one picture

One platform. Referral to report.

PEARL™ runs the process. AI supports the clinician's review: our own AiSPEED for colon capsule studies, the manufacturer's AI for other tests. Our service team handles kits and logistics.

  1. The provider orders the test, or a patient comes in through a partner clinician.
  2. A clinician checks that the test is right and safe, and gets consent.
  3. A SmartBox goes to the clinic or the patient's home, with prep instructions.
  4. The patient swallows the capsule. The recorder captures the study.
  5. The study comes back, is uploaded and checked for completeness.
  6. AI creates a complementary pre-read view: AiSPEED for colon capsule studies, the manufacturer's AI for other capsule tests.
  7. A clinician evaluates the whole study, using the AI pre-read as an additional view, and validates the findings.
  8. The signed report goes to the ordering physician, then to the patient.

Hover or tap a step for details

PEARLWorkflow, case tracking, kit logistics, study ingest from any capsule vendor
AI pre-readAiSPEED for colon capsule · manufacturer AI for other tests
ServicesSmartBox kits, courier and returns, reader network, training, support
GovernanceRole-based access, audit trail, quality management system, clinician accountability
Who does what

You deliver the care. We run the platform.

Ordering a capsule study becomes as easy as ordering a lab test or an X-ray.

Patient

Gets the test where it suits them

  • At home, a clinic or an imaging center
  • No sedation, no recovery time
  • Receives the report from their physician
Practice, imaging center or health system

Owns the clinical service

  • Selects and consents patients
  • Orders the test and owns the result
  • Reads and signs, or assigns a network reader
  • Bills under its own name
GI Digital

Supplies the platform

  • PEARL workflow and case tracking
  • AI-supported review in one workflow
  • SmartBox kits and logistics
  • Credentialed reader network on request

Who reads the study? The provider's own clinician, or a credentialed reader from the GI Digital network whom the provider assigns. Either way, the signed report goes to the ordering physician.

AiSPEED · colon capsule AI

AiSPEED pre-reads the full colon study.

A colon capsule study can contain tens of thousands of frames. Before the clinician opens it, AiSPEED creates a complementary pre-read view: anatomical landmarks, a bowel cleanliness assessment and marked frames that may contain relevant findings. The clinician evaluates the whole study, using the AI findings as an additional view. Validated findings can then populate a draft report for clinician review.

82%less reading timeUK multicentre study, 720 patients*

The AI does not make diagnostic decisions. The clinician remains responsible for evaluating the whole study and signing the report.

For small-bowel and other capsule tests, the platform uses the AI provided by the capsule manufacturer, integrated into the same GI Digital workflow.

Take the product tour
For patients

Your doctor doesn't offer it? You can still get it.

Talk to a licensed partner clinician by video. If the test is right for you, the kit comes to your door.

Proven in real programs

A decade of capsule operations.

National programs in Scotland and Denmark, NHS research in England, U.S. Tele-GI programs and the first capsule service on Guam.

See the evidence
Capsule endoscopy information table at the Guam Regional Medical City health fair
Experience across capsule platforms Medtronic ANX Robotica CapsoVision Jinshan Atmo Biosciences MiroCam

* CESCAIL, a multicentre UK study of AiSPEED-supported reading (720 patients enrolled). Results reported in peer-reviewed publications. AiSPEED had been CE-marked and UKCA-registered as Class I software. It is not FDA-cleared.