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About Medivdpharma (MIP)
At Medivdpharma (MIP), we are your dedicated strategic partner in bringing healthcare innovation to life. Specialising in medical devices, in-vitro diagnostics (IVDs) and pharmaceuticals, we offer integrated support across these interdependent domains—from concept through development, regulatory approval and commercial readiness. Our unique strength lies in delivering seamless and compliant pathways that accelerate market access, mitigate risk, and ultimately serve patients by improving and protecting human life.
Shapes
Shapes
Shapes

QMS Services

Audit Preparation

PMS data collection

Biocompatibility testing

Technical file writing

Clinical data collection

Training

UK rep and EU rep

Clinical Research

Headquartered in the United Kingdom, MIP operates internationally, supporting clients across the UK, Europe, Asia, the United States, and other global markets. Our deep expertise, extensive industry network, and proven strategic approach enable us to help organisations successfully navigate the pathways to global market access.
With significant experience in regulatory affairs, project management, and life sciences, we manage projects across a diverse range of sectors. Our dedicated team of experts works to streamline the entire process of bringing products to market — reducing risk, eliminating uncertainty, and ensuring full regulatory compliance.

We provide specialised support across a wide range of product categories, including:

  • Medical Devices
  • In Vitro Diagnostic (IVD) Devices
  • Combination Products
  • Pharmaceutical & Clinical Services
  • Combination Products

At MIP, our values form the foundation of our work: rapport, integrity, honesty, commitment, attention to detail, efficiency, and drive. We take the time to listen, understand, and analyse each client’s unique needs, ensuring we deliver tailored, effective strategies that accelerate market success.

Why Partner with MIP?
When speed, certainty, and expertise matter, trust MIP. We are the trusted global partner for bringing life-changing medical technologies to the world.
Our streamlined processes and proactive strategies cut through complexity to get your product to commercialization faster.
We integrate regulatory requirements from the initial concept phase, preventing costly missteps and ensuring confidence.
Our expert guidance helps you avoid expensive design changes and regulatory delays, protecting your investment.
From initial concept to manufacturing and post-market support, we are with you at every step of the way.