Medivdpharma Ltd – Bringing Medical Devices to Market, Faster

Developing a medical device is exciting, but the path to market can be complex. At Medivdpharma Ltd (MIP), we make it simpler. Our team of experts guides you through every step—turning regulatory challenges into a smooth journey from idea to approval.

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How We Help

We take care of the details so you can focus on innovation

Smart Regulatory Strategy

A clear plan to get your device approved in the markets you care about.

Device
Classification

Identifying the right risk class so you know exactly what’s required.

Technical Documentation

We prepare the DHFs, technical files, and evidence regulators demand.

Regulatory Submissions

From CE and UKCA marking to FDA 510(k), we handle the paperwork and process.

Quality Systems

ISO 13485–compliant QMS built to fit your business.

Training

Practical, tailored sessions to keep your team confident and compliant.

Post-Market Support

From audits to non-conformities, we’ve got you covered.

Why Choose MIP?

At MIP, your success is our mission. We turn complex regulations into a clear path forward helping you launch innovative, safe, and effective medical devices with confidence.

We don’t just check boxes—we build compliance into your device from the start. That means:

Faster time to market – Our streamlined process cuts delays.
Regulatory confidence – Approvals come smoother with compliance baked in.
Cost savings – Avoid the pitfalls that cause redesigns and rework.
User-centered design – Devices that feel intuitive for patients and healthcare professionals.
Full support – From concept to commercialization, we’re with you every step of the way.