PMCF Survey Drafting Expertise
For Your Device

Crafting your own survey guide? We can help integrate it into a PMCF Report.

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Unlock Compliance Excellence with Our Post Market Clinical Follow-Up Survey Solution for EU MDR & IVDR

Navigating the complexities of the European Union’s Medical Device Regulation (EU MDR) and In Vitro Diagnostic Regulation (EU IVDR) can be a daunting task for medical device manufacturers. The stringent regulations necessitate rigorous Post Market Clinical Follow-Up (PMCF) surveys, a challenge that demands precision, efficiency, and absolute compliance. Introducing our cutting-edge PMCF Survey Solution, designed to streamline this critical process, ensuring you not only save valuable time but also uphold the highest standards of regulatory compliance.

Comprehensive Survey Management, Simplified

Our innovative software platform is engineered to shoulder the burden of PMCF survey creation, distribution, and management.

Automated Survey Deployment

Craft detailed, regulation-compliant surveys with ease, and schedule their distribution with automated reminders. Our system is designed to respect your customers’ time and attention while maximizing response rates.

Real-Time Response Logging

Every interaction is captured and logged diligently in our secure platform, providing you with a detailed trail of documented evidence – a necessity under EU MDR and IVDR.

Insightful Dashboard Summaries

Stay informed and in control with our intuitive dashboard, offering a comprehensive summary of your ongoing campaigns, response rates, and key metrics, all accessible at a glance.

Start With Certainty

Save Time By Starting Right

Let your RA staff focus on the content that they know. With the structure set in place and annotations to guide you to a completed document.

Everything Included

Don’t risk missing/forgetting anything for your first submission.  Our Templates include everything you need for an EU MDR Audit

Updated Continuously

We constantly submit our own Templates, and update them based on the latest feedback from Notified Bodies.

Seamless CRM Integrations: Streamlining Your Workflow

We recognize the challenge: sales teams are reluctant to engage in activities that don’t align directly with their sales goals. Our solution? Seamless integration with leading CRM systems like Salesforce and Hubspot.

These integrations mean surveys can be triggered by actions within the CRM, removing the need for manual intervention by your salespeople. Although integrations are tailored and built case-by-case to suit your specific needs, the end result is a cohesive system that drives compliance activities forward without disrupting your sales processes.

Exclusive Access to Sourced Survey Data

We offer an invaluable “Sourced Survey Data” service. We don’t just wait for responses; we proactively tap into our extensive database of practitioners willing to provide insightful feedback on your devices. While the specifics of implementing this feature can be customized to your needs, the core idea remains: we bridge the gap between you and the firsthand feedback crucial for your PMCF obligations.

Your Compliance, Our Commitment

The stakes are high in the medical device field, and non-compliance isn’t an option. Our PMCF Survey Solution goes beyond a mere tool; it’s your strategic partner in fulfilling EU MDR and IVDR requirements. By automating and managing this intricate process, we free you to focus on what you do best: innovating in healthcare.

Don’t let the intricacies of compliance hinder your vision. With our platform, rest assured that your PMCF surveys are comprehensive, timely, and above all, compliant. Take a step toward uncompromised excellence and unwavering compliance today.

Have Questions?

Contact us to learn more about how our solution can be your cornerstone in EU MDR and IVDR compliance. Your commitment to healthcare excellence deserves a compliance process that reflects the same level of care and precision.

Let’s make it happen together.

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