Your Trusted Partner in IVD and Medical Device Development

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14

years of existence

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+1000 projects completed

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+15 clinical diagnostic areas

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50 collaborators

Cerba Xpert supports you in the IVDR steps

postmarket
Scientific Validity
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Analytical Performance
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Clinical Performance
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Post-Market Surveillance

An end-to-end solutions thanks to our belonging
to the Cerba Healthcare group, offering easy patients recruitment

Why choose Cerba Xpert ?

TImeline
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1
Title
Comprehensive Analytical & Clinical Services
Introduction

From study design to the Final Report through regulatory submissions, study setup, patient recruitment, study monitoring, and statistical analysis, Cerba Xpert provides a full suite of services tailored to your needs.

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2
Title
Regulatory Expertise
Introduction

Cerba Xpert ensures compliance with the stringent requirements of the EU IVDR 2017/746, helping you navigate the complex regulatory landscape smoothly.

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3
Title
Quality Assurance
Introduction

Cerba Xpert adheres to ISO 9001 and Good Clinical & Lab Practices rigorous quality management systems, ensuring the highest standards of data integrity and participant safety.