Grupo Alimentario S.A.
12 documents
Pacific Rim Foods Ltd.
9 documents
EuroGrain GmbH
15 documents
Andean Harvest Co.
7 documents
Sunrise Agri Corp
11 documents
The Platform
Everything your compliance team needs
DOSSA is the document intelligence layer that sits between your suppliers and the FDA — keeping every record current, every gap visible, every audit ready.
AI reads every document.
Drop in a PDF, image, or email attachment — DOSSA's AI extracts supplier, document type, expiry date, product, and more. No templates. No manual entry. Just upload.
- Reads COAs, certifications, specs, GFSI audits, and more
- Extracts expiry dates and alerts before they lapse
- Routes each document to the right supplier automatically
- Handles messy scans and non-standard formats
Requirements, tracked.
Define exactly which documents each supplier must keep current. DOSSA monitors every gap, flags expiring certs, and gives your team a clear action list — no spreadsheets needed.
- Custom document checklists per supplier or category
- Automatic expiry tracking with configurable alerts
- Gap reports exportable for audits
- Integrates with your FSVP evaluation schedule
A compliance control tower.
See the health of your entire supplier program in a single view. DOSSA surfaces risks, tracks corrective actions, and keeps you FDA-inspection-ready at all times.
- Live program health score across all suppliers
- Corrective action tracking and resolution logs
- Instant FDA-ready record exports
- Role-based access for your whole team
See it in action
Watch how DOSSA works
Start with the overview, then see the parts that matter to you.
A complete FSVP program, built in.
DOSSA's FSVP module delivers a fully documented Foreign Supplier Verification Program out of the box — covering every element of 21 CFR 1.500–1.514, so you're inspection-ready from day one.
Hazard analysis
Biological, chemical & physical hazard identification per 21 CFR 1.504
Supplier evaluations
Risk-based evaluation records for every foreign supplier
Verification activities
On-site audits, product testing, and document review logs
Corrective actions
Full corrective-action workflow with status tracking and timelines
FDA-inspection records
One-click export of all required records in inspection-ready format
Program documentation
All FSVP program documents stored, versioned, and searchable
Covers 21 CFR 1.500–1.514
Full FDA regulatory compliance scope
FSVP Program Dashboard
21 CFR 1.500–1.514 — FDA Ready
48
Suppliers
active
41
Evaluations
current
48
Hazard Analyses
complete
3
Open CAPAs
in progress
Foreign Supplier Verification
Supplier
Risk
Evaluation
Score
See if DOSSA is a fit.
Tell us about your operation and we'll show you exactly how DOSSA fits in.
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