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Turn Vision into Velocity with the Innovation CRO

Traditional CROs fragment device development with costly hand-offs and learning curves. Veranex unites the essential disciplines for medical device & diagnostic development under one roof from sketch to evidence-generation to market launch.

All connected. All aligned. All accelerating your path to market—delivering breakthrough devices and diagnostics that improve patient lives sooner.

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Outcome-Driven Solutions for Medtech Challenges

Breakthrough innovation requires more than great solutions; it demands deep expertise and insight. Veranex packages outcome-driven solutions with 25+ years of specialized knowledge across major medtech categories, delivering integrated capabilities that solve your most pressing challenges faster and with greater certainty.

Purpose-built solutions. Proven results. User & Patient-centered innovation.

 

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Purpose-Built for Breakthroughs

Whether you're transforming patient care or disrupting entire therapeutic categories, innovation requires more than great science, it demands velocity.  Veranex was founded to bridge the gap between visionary concepts and market reality, combining proven expertise with agile execution to accelerate the innovations that matter most.  

We are the Innovation CRO.

Legacy of excellence. Proven execution. Patient impact accelerated.

 

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Veranex Blog

EU IVDR

4 min read

Optimizing PLM-OEM Collaborations: Key Strategies for a Smooth IVDR Transition

Veranex: Dec 12, 2024 9:12:06 AM

Under Directive 98/69/EC (IVDD), it was common practice for in vitro diagnostic medical devices to be placed on the European market under contractual...

IVD Manufacturing Solutions EU IVDR
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3 min read

Amending Regulation for MDR / IVDR: Key Takeaways for the Diagnostics Industry

Veranex: Apr 26, 2024 9:41:14 AM

The EU Parliament adopted the regulation amending EU 2017/745 (MDR) and EU 2017/746 (IVDR) aiming to protect patients by ensuring the availability of...

EU MDR Regulatory EU IVDR
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4 min read

2024 IVDR Sprint: 6 Reasons Why You Should Start a Performance Evaluation Early

Veranex: Apr 17, 2024 7:33:47 AM

In accordance with Article 5(3) of Regulation (EU) 2017/746 (IVDR), a performance evaluation must be drawn up for every IVD placed on the European...

IVD Medical Writing EU IVDR
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2 min read

New Proposal for Extended Transition Periods for IVDs: Can Manufacturers Slow Down Transition Efforts? 

Joana Gomes: Jan 26, 2024 5:42:50 AM

On 23 January 2024, the EU Commission published a new proposal for amending the regulations EU 2017/745 (MDR) and EU 2017/746 (IVDR) aiming to...

IVD Regulatory EU IVDR
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