The Stripe for Digital Health

Ship lab-grade bloodwork in days, not a year

Aniva is the diagnostics layer for digital health builders. Order any of 2,500+ biomarkers as parameters, from a routine blood panel to whole-genome sequencing, through one REST API. Structured results, webhooks, and a live sandbox. The lab, the kits, the couriers and the compliance run behind it.

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API Docs for Developers
Powering diagnostics for

Trust and compliance

European standards, German precision.

The compliance set-up that is usually a four-month side project, included by default.

RiliBAEK

German lab quality regulation, covered by ZOTZ|KLIMAS

ISO 15189

Medical lab accreditation,
lab partner

GDPR

EU-native processing, AVV
included

EU-hosted

Germany-only infrastructure, full data sovereignty

MDR-aware

Aniva admin panel non-
qualifying under MDR/IVDR/MPDG

Anti-kickback

Sec. 299a StGB / Sec. 31 MBO-AE safe-harbour clauses
Why digital health platforms love Aniva

Diagnostics used to be the ugliest integration in health tech. That is the part we fixed.

Quickstart

From zero to a structured result in three calls.

Order a panel, listen for a webhook, read the result. You handle the product and the patient relationship. Aniva handles the lab, the sample logistics and the reporting underneath.

01

Order a panel

One POST creates the order and returns an id you can track. Pick any panel in the catalogue, or a custom one you defined.

POST /v1/orders
{ "panel": "complete_profile",
  "patient": "pt_8Q2f1a" }
02

Listen for the webhook

Every step, from sample drawn to lab complete, fires a signed event. No polling, no fax inbox, no guessing where the sample is.

# event: result.completed
{ "order": "ord_7642001142",
  "status": "completed" }
03

Read the result

Results come back as structured JSON with values, units and reference ranges, coded to standard lab identifiers. Render it, or embed the white-label view.

GET /v1/results/ord_7642
{ "marker": "ApoB",
  "value": 0.78, "unit": "g/L" }
Capability

From a single venous draw to whole-genome sequencing.

Aniva runs every modality routinely used in clinical and preventive medicine, plus most modalities that are not yet routine. Pick the panel your patients need, we handle the lab, the analytics, and the reporting.

Clinical chemistry

Routine bloodwork

Lipids, liver, kidney, glucose, electrolytes, full blood count, inflammation markers.

Tests
HbA1c
ApoB
Lp(a)
hsCRP
Cystatin C
GGT
ALT
Creatinine
Endocrinology

Hormonal panels

Thyroid, reproductive hormones, stress and adrenal axis, growth and IGF, prolactin.

Tests
TSH
fT3
fT4
Cortisol
Testosterone
Estradiol
SHBG
DHEA-S
Nutrient status

Vitamins and minerals

Vitamin and micronutrient status across the panels typical longevity and preventive medicine ask for.

Tests
Vitamin D3
B12
Holo-TC
Folate
Ferritin
Magnesium
Zinc
Omega-3
Immunology

Immune and autoimmune

Full immunoglobulin profile, autoantibodies, complement, allergen-specific IgE.

Tests
IgG/A/M/E
ANA
Anti-CCP
TPO
TRAK
C3/C4
Genetics

WGS, WES, polygenic risk

Whole-genome and whole-exome
sequencing, targeted panels, pharmacogenomics, polygenic risk scores.

Tests
WGS
WES
BRCA1/2
APOE
Pharmacogenomics
PRS cardio
Transcriptomics

RNA sequencing

Bulk RNA-seq and targeted transcriptomic panels, for emerging clinical and research questions.

Tests
Bulk RNA-seq
Targeted panels
Differential expression
Proteomics

High-throughput proteomics

Affinity proteomics and panel-based proteomic profiling via specialty partners.

Tests
Olink-style
Affinity panels
Inflammation
Cardiovascular
Microbiome

Routine bloodwork

16S and shotgun metagenomic sequencing, dysbiosis indices, and metabolite panels.

Tests
16S
Shotgun
Diversity
Metabolites
Loved by developers

Aniva is super easy to integrate

Everything a working integration needs is here on day one, built the way you would want it built, so your team can ship instead of firefight.

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A real REST API

Predictable resources, one Bearer key, JSON in and out, clear error objects. If you have called a modern API, you already know how this one behaves.

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Webhooks, not polling

Signed events for every status change: sample drawn, in transit, at the lab, completed. React in real time and keep your own UI in sync.

Idempotent by design

Send an Idempotency-Key and retry safely. A dropped connection never creates a duplicate order or a duplicate charge.

A sandbox with test data

Get a test key in minutes, order fake panels, and receive realistic result payloads. Build and demo the whole flow before a single real draw.

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Docs you will actually read

Copy-paste examples, every field described, live payloads. The kind of reference that answers the question before you open a ticket.

White-label patient views

Embed a branded results dashboard and PDF, or render the JSON yourself. Your logo, your colours, your domain. The patient never sees Aniva.

The Stripe-like Diagnostics API for Digital Health

Give your product lab-grade diagnostics it needs.

Request an API key and try the sandbox with a 20-minute technical intro to see the endpoints, the webhook flow, and a real contract with your engineers in the room.

Lp(a
Fasting Insulin
Uric Acid
Homocysteine
Folate (RBC)
Ferritin
TSH
SHBG
GGT (liver)
Magnesium
Whole-genome sequencing
Whole-exome sequencing
Polygenic risk - cardio
BRCA1/2
Pharmacogenomics
APOE genotype
ApoB)
HbA1c
Cystatin C
hsCRP
Vitamin D3
Omega-3 Index
Holo-TC / B12)
Free Testosterone
 Estradiol
Magnesium
Whole-genome sequencing
Whole-exome sequencing
Polygenic risk - cardio
BRCA1/2
Pharmacogenomics
APOE genotype
ApoB)
HbA1c
Cystatin C
hsCRP
Vitamin D3
Omega-3 Index
Holo-TC / B12)
Free Testosterone
 Estradiol
Magnesium
Whole-genome sequencing
Whole-exome sequencing
Polygenic risk - cardio
BRCA1/2
Pharmacogenomics
APOE genotype
Lp(a
Fasting Insulin
Uric Acid
Homocysteine
Folate (RBC)
Ferritin
TSH
SHBG
GGT (liver)
Magnesium
Whole-genome sequencing
Whole-exome sequencing
Polygenic risk - cardio
BRCA1/2
Pharmacogenomics
APOE genotype
Lp(a
Fasting Insulin
Uric Acid
Homocysteine
Folate (RBC)
Ferritin
TSH
SHBG
GGT (liver)
Magnesium
Whole-genome sequencing
Whole-exome sequencing
Polygenic risk - cardio
BRCA1/2
Pharmacogenomics
APOE genotype

More than two thousand five hundred parameters available