MedStride was founded by Dr Benyamin Rahmani, a former Reviewer and CE/UKCA Scheme Manager at BSI. Having worked with the world’s leading medical device companies and emerging innovators alike, we bring regulatory insights, strategic perspective, and practical clarity to every engagement.
Plan for success with expert guidance on device classification, intended purpose, and appropriate conformity route.
Build compliant technical documentation, including risk management, clinical evaluation, and design verification.
Get support for certification submissions, audits, gap assessments, and ongoing regulatory compliance.
We work with manufacturers across all device classifications, from low-risk products to complex implantables.
Our experience includes cardiovascular and structural heart technologies. We bring a level of insight and precision that helps manufacturers avoid delays, and strengthen their documentation from the start.
Our approach combines regulatory insight with clear, practical guidance. We work closely with regulatory, clinical, and engineering teams to simplify complex requirements, strengthen your documentation, and support smooth certification.
We work with medical device manufacturers from anywhere in the world seeking entry into the EU and UK markets. You’ll receive support tailored to your device, conformity route, and regulatory goals.
Drop us a line to discuss your challenges, and find the most efficient path toward.
