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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

2 min read

Prioritizing Patient Safety and Fostering Innovation with the MHRAs New Roadmap for Medical Devices

Veranex: Mar 8, 2024 9:15:15 AM
Data Management Device CRO Safety
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4 min read

Strategies for Successful Clinical Data Management Rescue Studies

Veranex: Mar 5, 2024 5:03:46 PM
Data Management Device CRO Trial Strategy
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3 min read

Implications of FDA’s Quality Management System Regulation (QMSR) Final Rule

Veranex: Feb 21, 2024 12:16:08 PM
FDA Regulatory Quality Product Development
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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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3 min read

The Role of Scientific/Medical Literature Screening and Review in Pharmacovigilance

Heidi Jerman: Nov 29, 2023 4:16:41 PM
FDA Regulatory Quality Medical Writing
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2 min read

Key Insights from NMPA Guidance Draft 01 & 02 from Our Human Factors Team

Veranex: Nov 14, 2023 3:14:22 PM
Human Factors Device Design
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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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5 min read

Challenges for Medical Device Database Builds and Strategies to Overcome Them

Veranex: Sep 13, 2023 3:51:59 PM
Data Management Device CRO
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5 min read

Biocompatibility of Medical Devices: Process, Detailed Steps and 7 Hot Topics to Crack the Code of Medical Device Safety

Picture of Neeru Mittal, PhD Neeru Mittal, PhD: Sep 13, 2023 6:07:09 AM
Biocompatibility Product Development Device CRO
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4 min read

Deriving Value From Strategic Relationships and Tailored Solutions: Our Takeaways From PCT Summit – Amsterdam 2023

Veranex: Apr 21, 2023 4:20:42 PM
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