Veranex
★★★★★
3.8
/ 5
•
12 reviews
Veranex is a leading provider of data-driven solutions for go-to-market strategies. They empower sales and marketing teams with comprehensive data and insights to drive revenue growth and market success.
Veranex offers a robust platform designed to unify teams, strategies, and data-driven technologies, enabling businesses to convert leads at the speed of demand. Their solutions provide foundational data and buying signals, connecting industry-leading data across your entire tech stack. With a focus on enabling sales and marketing operations, Veranex helps organizations discover their next best customer, track key contacts, and prospect the entire buying committee. Their platform is built to deliver insights and data on your terms, ensuring that strategy turns into execution and sales teams can hit their numbers more effectively. Leveraging advanced features like ZoomInfo Copilot and GTM Workspace, Veranex supports a modern go-to-market approach. They are committed to helping over 30,000 customers find, acquire, and grow their customer base, making them a strategic partner for revenue growth.
About
**Who they are**
Veranex is an Innovation CRO that unites essential disciplines for medical device and diagnostic development under one roof, from concept to market launch. They leverage over 25 years of specialized knowledge across major medtech categories to accelerate innovations that improve patient lives.
**Expertise & scope**
* Integrated capabilities for medical device and diagnostic development.
* Expertise in QMS implementation and audit readiness.
* Services to prevent regulatory setbacks and accelerate market entry.
* Specialized knowledge in areas including Research & Strategy, Product Design, Software Development, Engineering & Development, Testing & Prototyping, Human Factors, Manufacturing Solutions, Non-GLP Preclinical, GLP Preclinical, and Surgical & Bioskills.
* Designation as an EU Authorized Representative for non-EU manufacturers, fulfilling legal requirements for regulatory compliance and vigilance reporting within the European Union.
**Reputation / proof points**
* Over 25 years of specialized knowledge across major medtech categories.
* Focus on user & patient-centered innovation.
* Combines proven expertise with agile execution.
Veranex is an Innovation CRO that unites essential disciplines for medical device and diagnostic development under one roof, from concept to market launch. They leverage over 25 years of specialized knowledge across major medtech categories to accelerate innovations that improve patient lives.
**Expertise & scope**
* Integrated capabilities for medical device and diagnostic development.
* Expertise in QMS implementation and audit readiness.
* Services to prevent regulatory setbacks and accelerate market entry.
* Specialized knowledge in areas including Research & Strategy, Product Design, Software Development, Engineering & Development, Testing & Prototyping, Human Factors, Manufacturing Solutions, Non-GLP Preclinical, GLP Preclinical, and Surgical & Bioskills.
* Designation as an EU Authorized Representative for non-EU manufacturers, fulfilling legal requirements for regulatory compliance and vigilance reporting within the European Union.
**Reputation / proof points**
* Over 25 years of specialized knowledge across major medtech categories.
* Focus on user & patient-centered innovation.
* Combines proven expertise with agile execution.
Additional information
Veranex acts as a crucial EU Authorized Representative, fulfilling the legal mandate for non-EU manufacturers to have a designated entity within the European Union. This service is critical for ensuring ongoing medical device regulatory compliance and managing vigilance reporting. Their approach integrates technical documentation management and regulatory strategy to address market access challenges effectively. By providing continuous regulatory support, they help manufacturers navigate the complexities of the European market, ensuring safety oversight and timely communication with authorities.
Key Highlights
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Veranex unites essential disciplines for medical device & diagnostic development under one roof from sketch to evidence-generation to market launch.
Source
“Veranex unites the essential disciplines for medical device & diagnostic development under one roof from sketch to evidence-generation to market launch.”
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They offer comprehensive EU Representation Services, including regulatory compliance, documentation, market access, and vigilance oversight.
Source
“Comprehensive EU Representation Services; Regulatory Compliance & Documentation; Market Access & Monitoring; Vigilance & Safety Oversight”
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Leverages over 25 years of specialized knowledge across major medtech categories.
Source
“Veranex packages outcome-driven solutions with 25+ years of specialized knowledge across major medtech categories”
Certifications & Trust Signals
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Veranex positions itself as the 'Innovation CRO', accelerating the path to market for breakthrough devices and diagnostics.
Source
“We are the Innovation CRO.Legacy of excellence. Proven execution. Patient impact accelerated.”
Buyer Snapshot
Best for
- Non-EU medical device manufacturers seeking EU representation.
- Companies needing integrated support from development to market launch.
How engagement typically works
- Strategic partnership for regulatory compliance.
- Outcome-driven solutions with deep expertise.
Typical deliverables
- EU Authorized Representative services.
- Regulatory compliance and vigilance reporting.
- Technical documentation management.
- Market access and monitoring support.
Good to know
- Best when requiring specialized medtech development and regulatory expertise.
HQ:
Vancouver, US
Languages:
English, French
Timezones:
Europe/Paris
Claim status:
Listed
Services & Capabilities
Find EU Authorized Rep (EC REP) | Compare & Get Quotes
Jurisdictions:
EU
Countries:
FR, BE, NL, DE, IE, ES, IT
Industries:
Medical devices, IVD, Healthcare
Portfolio:
26-100, 100+
Onboarding time:
3–21 days
Pricing model:
Custom pricing
Starting from:
EUR 9,000
Included services:
EU Authorized Representative (EC REP) designation, Authority liaison and document availability support, Vigilance escalation and FSCA coordination, Labeling/EC REP identification review, Post-market support workflows (complaints, vigilance escalation)
Supports MDR:
Yes
Supports IVDR:
Yes
Post Market Support:
Yes
Labeling Review:
Yes
Vigilance Contact Support:
Yes
Fsca Recall Support:
Yes
EU Entity Country:
EU
Additional eu_ar Details
Supports MDR
true
EU Entity Country
EU
Fsca Recall Support
true
Post Market Support
true
Vigilance Contact Support
true
Onboarding Steps
The process involves fulfilling legal requirements for non-EU manufacturers to have designated representation within the European Union for medical device regulatory compliance and vigilance reporting, supported by technical documentation management and regulatory strategy.
Supports IVDR
Yes
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