Haven

Data sources

Every signal in Haven traces back to a named source.

Haven aggregates regulatory, public reference, and supplier-provided data. Each source is labeled with what it informs, how often it refreshes, and the caveat a reviewer should keep in mind.

Health Canada DPDFDA / openFDADailyMedEMARxNormHealth Canada ShortagesSupplier documentation
Source matrix
Source
Type
What it informs
Refresh
Review caveat
Health Canada DPD
Regulatory
Canadian market authorization, DIN matching, product status.
Weekly
Authoritative for CA authorization; confirm current product status.
FDA / openFDA / DailyMed
Regulatory
US approvals, structured product labeling, adverse-event context.
Daily
US scope; verify the current label revision before relying on it.
EMA
Regulatory
European centralized authorizations and product information.
Weekly
Centralized procedures; national status may differ by member state.
RxNorm
Reference
Normalized drug naming and cross-source identifier mapping.
Monthly
A naming aid for matching — not a market-approval source.
Health Canada shortages
Public
Shortage and discontinuation signals informing sourcing urgency.
Daily *
Advisory; reporting reflects submissions, not real-time stock.
Supplier documentation
Supplier
GMP status, provenance, listing detail, and compliance files.
On submission
Supplier-attested; requires verification through Haven review.
* Drug-shortage ingestion is on the roadmap; cadence shown is the planned target.
Confidence & freshness

We show how much weight a signal can carry.

Each record surfaces its source run status and a confidence level, so reviewers can tell authoritative regulatory data from supplier-attested or advisory input.

High
Authoritative regulatory
Direct match to an official database record, recently refreshed.
Moderate
Needs verification
Partial match, stale refresh, or supplier-attested documentation.
Unknown
No reliable match
Insufficient source data; flagged for human review before use.

Regulatory, clinical, supplier, and landed-cost information is provided for procurement review and must be verified before procurement, importation, distribution, or clinical use.

Review & provenance →