Defense · GMLP
GMLP for defense AI workflows
GMLP in defense AI workflows: what compliance requires, who asks for evidence, and the records to keep.
01 / The rule
What GMLP requires
Manufacturers developing AI/machine-learning-enabled medical devices for the US, Canadian and UK markets, and the regulators reviewing them.
- 01Use multidisciplinary expertise throughout the total product lifecycle and follow good software engineering and security practices.
- 02Use clinical study participants and data sets representative of the intended patient population.
- 03Keep training data sets independent of test sets, and base reference datasets on best available methods.
- 04Tailor model design to the available data and intended use, and evaluate performance of the human-AI team.
- 05Test device performance under clinically relevant conditions and give users clear, essential information.
- 06Monitor deployed models for performance and manage retraining risks.
02 / In this sector
In a defense AI workflow
AI-specific. The principles were written for medical devices that use machine learning, including models that are retrained or updated after release.
Program office leads and ATO-package owners.
NIST AI RMF · DoW RAI · OMB M-25-21.
03 / Records
Records to keep
- 01Dataset documentation showing representativeness and train/test separation
- 02Reference standard (ground truth) method and rationale
- 03Clinical performance testing report under intended-use conditions
- 04Post-market performance monitoring plan and retraining change records
Optional evidence · where Planisphere fits
Keep a record anyone can check
When your team meets a duty, Planisphere can seal the event it reports as a receipt.
A disclosure shown, a review signed, a model change approved: the event your system reports.
The event becomes a sealed receipt, dated and attributed to whoever is signed in.
Paste the receipt into Verify. No account or key.
A record supports your compliance evidence process. It is not a legal finding or a certification. Systems that call Planisphere's gate API can also hold or refuse an action before it runs.
SOURCES
Go back to the source
Medicines and Healthcare products Regulatory Agency (GOV.UK)
U.S. Food and Drug Administration
International Medical Device Regulators Forum
Regulatory Affairs Professionals Society
RELATED
Related: GMLP: the full guide · GMLP for medicine · GMLP for law · GMLP for education