Medical Device & Pharma

Supplier Compliance for
Regulated Medical Products

VendorWeave automates MDR materials declarations, tracks ISO 13485 and FDA certifications, manages risk-based onboarding, and scores supplier performance — built for teams that answer to auditors.

See It In Action

Track ISO 13485, FDA, and MDR compliance in one dashboard

Live Dashboard
VendorWeave compliance dashboard tracking ISO 13485, FDA, and MDR certifications

Real-time visibility into supplier certifications with automated expiration alerts

Built for Medtech Compliance Challenges

MDR materials declarations stuck in email threads for weeks

Automated MDR Annex I survey collection with AI parsing and deadline tracking

ISO 13485 and FDA registration certs expire without anyone noticing

10-day and 5-day expiration alerts with automated renewal requests to suppliers

Supplier onboarding takes 6+ weeks with manual document chasing

Risk-based onboarding workflows with auto-reminders — high-risk suppliers get the full package automatically

Quality events (CAPAs, complaints) scattered across spreadsheets and email

Centralized quality log with CAPA, SCAR, and complaint tracking tied to supplier scorecards

Regulatory Coverage

VendorWeave tracks the certifications and declarations your auditors ask for.

EU MDR 2017/745 — Materials declarations (Annex I)
FDA 21 CFR Part 820 — Quality System Regulation
ISO 13485 — Medical Device QMS
ISO 14971 — Risk Management
RoHS & REACH — Substance compliance
Conflict Minerals (Dodd-Frank) — 3TG reporting

What Medtech Teams Use Most

Compliance Tracking

ISO 13485, FDA, MDR, RoHS, REACH — all in one dashboard with expiration alerts.

Supplier Scorecards

Five-metric scoring tied to quality logs. Know which suppliers are improving or declining.

Quality Management

CAPAs, SCARs, and complaints tracked per supplier with full audit trail.

Ready to automate medtech compliance?

Start free with 5 suppliers. All compliance features included. No credit card required.