Eliminate supplier delays and get products to market faster.
Graphite’s lightning-fast supplier management keeps vendors moving through your GxP compliance and quality checks to create an auditable source of truth that quality and risk teams love.
Compliance Without Compromise: Accelerating Innovation Safely
In the highly regulated Pharma and Med Device industries, every minute spent on manual supplier vetting, document chasing, or risk assessment delays life-saving products.
Graphite provides the single, validated source of truth your procurement, quality, and compliance teams need to move with unprecedented speed and confidence.
Fast Supplier Collaboration to Deliver GxP Excellence
Bad supplier data is holding you back.
In our 2026 State of Supplier Data white paper, learn the key challenges in building a supplier master data management strategy and how it’s killing the ROI on your AI investments.
Unlock total transparency for stakeholders
Every step of your process is clear to the teams following the project’s success and delivery timelines. Quality, Compliance, Legal, Supply Chain teams know who is next up to bat in reviewing and approving suppliers, keeping you on track and preventing project delays.
Every supplier contact at your fingertips.
Frequently Asked Questions (FAQs)
What is pharmaceutical and medical device vendor management?
Pharmaceutical and medical device vendor management is the process of onboarding, validating, risk-assessing, and continuously monitoring the suppliers that feed regulated manufacturing and quality processes. In GxP environments, it requires a validated, auditable source of truth for supplier certifications, quality documents, and commercial data so quality, compliance, and procurement teams can move quickly without sacrificing regulatory readiness.
How does Graphite help pharma and med device companies stay compliant with GxP, FDA, and EU MDR?
Graphite centralizes supplier certifications, quality documents, and tax forms into a single validated profile and maintains an audit-ready documentation repository. The platform supports customizable assessment workflows and automated sanctions screening, helping teams navigate FDA, EU MDR, and other global regulations while keeping every step of the review and approval process transparent and traceable.
How does Graphite speed up supplier onboarding in regulated industries?
Graphite eliminates duplicate data entry by consolidating all necessary supplier information into one validated profile, drastically reducing onboarding time and ensuring regulatory readiness from day one. Instead of reconciling disparate data systems and chasing documents, teams work from a single source of truth that accelerates time-to-market.
What is third-party risk management (TPRM), and how does Graphite handle ongoing risk assessments?
Third-party risk management (TPRM) is the practice of identifying and mitigating the risks a supplier introduces to your business. Graphite automates both initial and recurring third-party risk assessments, screening suppliers against international sanctions and validating their commercial information, so risk reviews happen continuously rather than as one-time checks.
How does Graphite monitor supplier performance and quality?
Graphite provides continuous performance management through custom KPI tracking and alerting, monitoring metrics like quality scores, responsiveness, and delivery. It automatically flags underperforming or high-risk suppliers and supports structured Supplier Action Plans (SAPs), enabling proactive intervention before issues disrupt the supply chain.