KERNEL

Draft your Protocols

The first draft, written by KERNEL. Traced to source, ready for human review.

Layer 1: Source Aggregation
PubMed
347 publications
EMA
ICH Guidelines
ANSM
Safety Alerts
ClinicalTrials
Trial Registry
Internal Data
Sponsor Studies
Scientific Data
Warehouse
5 sources · 892 documents indexed

Your Scientific Data Warehouse

PubMed, EMA, ANSM, ClinicalTrials.gov and your proprietary data, aggregated, structured, and queryable in seconds.

From first draft to submission, without losing the source.

KERNEL writes the first draft. Your teams verify, annotate, approve. Every sentence stays traceable back to its original source.

What our users say

Literature review is no longer a bottleneck. My medical teams get an exhaustive, up-to-date view of the science for every trial in minutes.

Medical Director

Our review and validation cycles went from several weeks to a few days. Every source stays traced, verifiable, ready for compliance.

Head of Regulatory Affairs

Drafting a CSR used to take us two weeks on average, with heavy data-control follow-up. KERNEL cuts that by 60% without sacrificing rigor.

Clinical Project Manager

Frequently asked questions

Let's meet

See how KERNEL fits into the drafting of your clinical trial documents.