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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 MDR

4 min read

From MDR Irritation to ISO 10993-1:2025 Advantage: Your Path Forward

Picture of Lina Burman Lina Burman: Jan 19, 2026 6:00:00 AM
EU MDR FDA Regulatory Biocompatibility
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2 min read

ISO 10993-1:2025 Questions Medical Device Innovators Should Answer

Picture of Lina Burman Lina Burman: Nov 25, 2025 4:00:00 AM
EU MDR FDA Regulatory Biocompatibility
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4 min read

Understanding Clinical Evaluation as an Early Strategic Process, Not Just Last-Minute Paperwork

Picture of Julianne Bobela, PhD Julianne Bobela, PhD: Nov 19, 2025 7:30:00 AM
EU MDR Clinical Research EU IVDR
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5 min read

ISO 10993-1:2025 Publication Is Imminent: Implications for Med Device Innovators and Manufacturers Worldwide

Picture of Lina Burman Lina Burman: Oct 22, 2025 8:23:33 AM
EU MDR FDA Regulatory Biocompatibility
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4 min read

eQMS (Software) vs. a Scalable, Compliant, High Value QMS: Know What You're Buying

Picture of Ramona Field Ramona Field: Sep 30, 2025 6:14:08 PM
EU MDR FDA Regulatory Quality
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4 min read

The Market Shift to In-Home Care: Navigating New Challenges and Opportunities for Medical Devices at Home

Picture of Jess Willing-Pichs Jess Willing-Pichs: Sep 24, 2025 10:24:05 AM
EU MDR Product Development Device Design
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1 min read

Critical Updates for Medical Device Manufacturers and Healthcare Institutions: Switzerland Aligns with EU IVDR Transitions

Veranex: Jan 17, 2025 12:28:45 PM
EU MDR IVD
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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
EU MDR Regulatory EU IVDR
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5 min read

Artificial Intelligence (AI), General Data Protection Regulation (GDPR) and Cybersecurity: 10 Misconceptions About Medical Device Software

Veranex: Mar 13, 2024 5:27:29 PM
EU MDR Software Development AI
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5 min read

Medical Device Vigilance: Important Considerations to Comply With the EU MDR

Veranex: Apr 7, 2023 4:34:31 PM
EU MDR Quality Safety
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