Two ways to reach us
Most enquiries land in one of two buckets. Pick the one that fits.
Applying as a regulatory expert? Go straight to our experts page — that route is separate.
Book a Demo
See the platform in action. Book a free 20-minute walkthrough and we'll show you how PraxisVerify reduces expert engagement from months to hours. During the demo, we'll walk through the secure document review workflow, show you how expert matching works, and explain how the audit trail is designed to support 21 CFR Part 11 requirements.
Whether you're preparing for an FDA submission, need a Clinical Evaluation Report reviewed, or want to see how platform credentialing replaces vendor qualification, the demo is tailored to your use case.
Book a 20-min DemoClient Enquiries
We welcome enquiries from MedTech manufacturers, pharmaceutical companies, and other life sciences sponsors. Whether you have a question about the platform, want to discuss a specific compliance challenge, or are interested in partnership opportunities, get in touch.
We aim to respond within one business day. For urgent matters, please include "Urgent" in your subject line.
linkedin.com/company/praxisverify
Connect with PraxisVerify for regulatory updates and life sciences compliance discussion.
For Regulatory Experts
If you're a regulatory professional considering joining the PraxisVerify expert network, the expert journey runs through a separate page — with the credentialing model, scope, rates, insurance, and conflict of interest workflow set out in full.
Common Use Cases
Companies typically reach out when they need expert support for:
- FDA 510(k) submission review — pre-submission technical documentation verification by a regulatory specialist with FDA experience.
- EU MDR Clinical Evaluation Report (CER) review — clinical data appraisal and literature review validation by an experienced assessor.
- ISO 13485 gap analysis — third-party QMS assessment by a qualified lead auditor ahead of certification or surveillance audits.
- Design History File (DHF) verification — independent review of design inputs, outputs, verification, and validation records.
- Post-market surveillance — vigilance report assessment and PMCF strategy validation for ongoing EU MDR compliance.
Not sure which service fits your needs? Book a demo and we'll help you scope the engagement.
Location
PraxisVerify Ltd
Ireland
At the heart of Europe's life sciences hub — home to 9 of the world's top 10 pharmaceutical companies (IDA Ireland) and a thriving MedTech sector. Ireland's strong regulatory ecosystem, combined with its position as a European base for medical device manufacturers and contract research organisations, makes it the ideal home for a platform serving global life sciences compliance.
The global medical device market was valued at approximately $595 billion in 2024 and is projected to reach $893 billion by 2032 (Fortune Business Insights, 2025). As regulatory complexity increases — with the EU MDR transition affecting over 25,000 existing CE-marked devices and the FDA processing approximately 3,500 510(k) submissions annually — demand for qualified, independent expert review continues to grow.