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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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Turn Our Insights Into Your Impact

From early feasibility to commercialization, progress depends on the right decisions at the right time. Get confident in your next step with blogs, case studies, and expert insights that cut through complexity and move development forward.

 

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Veranex Blog

Regulatory (2)

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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4 min read

Built to Fit Your Needs: Our CDMO Capabilities

Picture of Bill Croisetiere Bill Croisetiere: Mar 19, 2024, 11:50:38 AM
Manufacturing Solutions Quality Regulatory
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2 min read

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

Veranex: Jan 26, 2024, 5:42:50 AM
IVD Regulatory EU IVDR
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5 min read

Nanomaterials in Medical Devices: Biological Risks and Methodology for Biocompatibility Assessment

Veranex: Sep 28, 2023, 4:05:23 AM
Biocompatibility Safety Regulatory
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3 min read

Agile vs. Regulatory: How the Two Coexist and Contribute to Successful Medical Device Software Development

Picture of Nuria Gresa, PhD Nuria Gresa, PhD: Feb 27, 2023, 3:59:29 PM
Software Development Quality Regulatory
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2 min read

Basics of Drug Safety: Importance of Case Processing in Pharmacovigilance (PV)

Veranex: Feb 9, 2023, 4:08:56 PM
Biopharma Safety Regulatory
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2 min read

The New Normal for Market Access in China: Volume Based Procurement

Gary Keeler: Jan 17, 2023, 9:33:14 AM
Commercialization Regulatory
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2 min read

Medical Writing in Early Phase Studies

Veranex: Jul 5, 2022, 11:38:45 AM
Medical Writing Regulatory
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2 min read

FDA Releases Final Guidance on Oncology Therapeutic Class Labeling of Companion Diagnostics

Veranex: Apr 21, 2020, 12:43:18 PM
IVD FDA Regulatory Regulatory
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1 min read

The VALID and VITAL Acts: What Do They Mean for Diagnostic Innovators?

Veranex: Apr 6, 2020, 12:45:46 PM
IVD FDA Regulatory Regulatory
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