A team that truly understands both clinical practice and data. We are not data movers: we govern dormant raw records inside hospitals into data assets that can be trusted, authorised and used for training.
Many data companies assemble their capabilities from generic technology stacks. Our difference is the order of things: devices and clinical settings came first, and data standards followed — because only by knowing which parameters clinicians truly care about can you know what deserves governance.
We govern heterogeneous data from HIS / EMR / LIS / PACS into data assets with consistent definitions, traceable lineage and controllable sensitivity.
Turning clinical experience into quantifiable gold-standard datasets — through a process that is itself auditable and reproducible.
We focus on the two areas where we genuinely master clinical semantics, make no generalised promises, and build only models that can be validated.
Turning medical data from records sitting in a server room into assets with defined rights, a pricing basis and compliant delivery.
Medical data is not a business a single-background team can run. Our staffing deliberately covers four capabilities — clinical, data, compliance and engineering. Without any one of them, nothing works.
All of the above are delivered as working implementations covered by automated tests, and can be demonstrated live during a technical discussion.
Rather than a generic capability list, here are the four types of engagement we can take on directly, and what we deliver in each.
Building data governance systems and disease-specific databases for hospitals: data inventory, standards alignment, quality governance and compliance assessment — producing real-world data assets usable for research and clinical work.
Delivery: governance plan + disease-specific database + data asset ledger + compliance evidence chainTaking on disease-specific dataset annotation projects and delivering gold-standard datasets that meet QC standards; or jointly running model training, evaluation and multi-centre external validation with research institutions.
Delivery: gold-standard dataset + dataset card + validation reportHelping hospitals define data asset rights, aggregate costs and assess registration, and engaging compliant data exchanges to complete the full process from listing to delivery and settlement.
Delivery: rights evidence pack + assessment basis + transaction delivery certificatesProviding integrated device and data solutions for maternal and child health hospitals, fertility centres, and postnatal and aesthetic clinics, capturing the care process as usable data assets under compliance.
Delivery: device solution + data ingestion + follow-up management systemFirst establish data entry points through compliant products, then build data assets through governance and annotation, and finally bring disease-specific models and agents into daily clinical practice.
The credentials below can all be verified through official channels; original certificates are available to partners on request.
The medical ozone therapy device holds National Class II medical device registration and is qualified for nationwide market access.
Class II medical device distribution filing has been completed, with a business scope covering the relevant catalogue categories.
Filing number: 苏常药监械经营备20240154号The Chinese brand "安必特" and the English brand "Armeebeauty" are both registered, approved for Class 10 medical device goods.
安必特 No. 76761750 · Armeebeauty No. 73776559The core control system software has been registered for computer software copyright.
Medical Ozone Therapy Device System Control Software V1.0 · 2026SR0627822A quality management system is established and operating, covering R&D, production, inspection and after-sales service.
Multiple core patents covering ozone generation, concentration control, magnetic field regulation and catheter structure.
We welcome partners to visit our Changzhou headquarters to see our products, production lines and quality system first-hand.
