You may be in one of these situations
Your investigator brochure needs updating before the next submission
The deadline is six weeks away. You need to integrate 18 months of new publications, update safety data, verify nothing has changed on the regulatory side. One person is working on it full-time.
With KERNEL, publications and regulatory data are already aggregated. The update starts from a complete picture, not a blind PubMed search.
You're launching a new trial and the protocol needs to be ready fast
The design is validated, the scientific committee has decided. Now you need to produce an 80-page protocol backed by literature. Your medical writer is already on another project.
With KERNEL, a structured, sourced first draft ready for review. Your writer focuses where they add the most value: scientific judgment.
You're preparing a regulatory submission and time is running out
Three CTD modules to finalize, a CSR under review, inconsistencies between documents. The team is working weekends.
With KERNEL, every claim is traced to its source, cross-document inconsistencies are detected, team review is structured. The dossier moves forward without last-minute surprises.
You're a CRO and every project has its own constraints
Different clients, different formats, different requirements. Your writers spend as much time searching for information as writing.
With KERNEL, over 30 sources centralized in a warehouse searchable in seconds. Your teams write instead of searching.