Propel for Medical Devices

Improve patient outcomes by enhancing quality while reducing corporate risk.

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Get compliant, then stay compliant — all while improving product and service quality

Medical device companies must navigate changing global regulations while building and maintaining great products. All this, while improving the lives of patients. We can help.

Design and produce best-in-class products

Remove silos between departments and systems to seamlessly deliver products from concept to customer.

Achieve and maintain compliance

Manage and publish localized electronic Instructions for Use (eIFU); manage Digital FDA submissions by gathering information directly from product and quality records to create, submit, and track MedWatch Form FDA 3500.

Closed-loop quality management

Build quality into new products, manage non-conformances and supplier quality, and seamlessly address customer issues by linking cases to complaints to the product record.

Manage market entry  and distribution

Create, track, and renew product registrations across all your global markets with our Global Product Registration capabilities. CRM and ERP integrations ensure compliance with local distribution rules and enable region-specific stop shipments as needed.

Benefits of Propel for Medical Devices

Improve patient outcomes

Develop and launch impactful, high-quality products, deliver superior service, and rapidly resolve customer complaints.

Secure ongoing revenue

Maximize revenue and extend to new markets by complying with local regulatory agencies across the globe, including the FDA, EU-MDR, and MDSAP.

Mitigate risk

Proactively manage risk through timely and complete adherence to regulatory mandates.

Close the loop on one platform

Propel is the only product success platform built on Salesforce that creates a closed-loop system with unparalleled capabilities.

Fully-validated QMS

Use Propel as a quality management system for any classification device with the ability to pull releases on your own schedule.

Integrated PLM and QMS

Quality starts with design and development when you integrate PLM and QMS, reducing future costs, better patient outcomes, and less customer service issues.

Customer 360 + Product 360

Resolve complaints faster, automate stop-ship orders, and automate electronic instructions for use with extensibility to Salesforce Sales Cloud, Service Cloud, and Community Cloud.

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Success stories from med tech customers

You can do just about anything in Propel. It is very quick and very snappy.

Brian Beach

Project Engineer, Yukon Medical

We needed a solution that could adapt to us versus us adapting to them. With Propel we can mistake-proof our processes to gain business efficiencies and at the same time ensure compliance.

Brent Lewis

Director of Enterprise IT Quality and Compliance Systems, ASP

The combination of PLM and QMS was huge for us. We can now track product and component problems all the way back to the PLM structure of the items to see if that item has been related to a quality incident. Propel gives the engineer immediate visual access to those quality issues.

Donielle Baudin

Director of QA, Imperative Care

Resources for med tech


Deliver Better Patient Outcomes with Company-Wide Collaboration

Hear quality experts explore why quality and design teams are embracing platform consolidation as the best way to eliminate gaps and white spaces, unify data, and streamline business processes.

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Case Study

ASP Case Study

Advanced Sterilization Products (ASP) had quality management processes in place that were previously spread across multiple systems. Propel provides them with an integrated solution for all of their product and quality information.

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Benefits of Closing the Loop Between Quality and Product Development

A collaborative, closed-loop system for managing both product development and quality helps medical device manufacturers improve the lives of patients and reduce corporate risk.

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Ensure Compliance Across the Product Lifecycle

Maintain compliance with a unified platform that records and connects all document management and quality processes to the product record.

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