

Your Partner in Regulatory and Clinical Affairs
for Medical Innovation
â„“ Pharmaceuticals â„“ Medical Devices â„“
What is ORPHAN QUANTUM ?
With ORPHAN QUANTUM, I offer specialized services in regulatory, clinical, and scientific support for healthcare innovation stakeholders. I work with pharmaceutical companies, biotechs, and medtechs to help them progress in their operations, from preclinical to post-market stages, in Europe and internationally.
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As an independent consultant, I provide tailored operational support based on a strategic understanding of your development challenges, precisely adapted to your projects.
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My goal is to help you transform regulatory and scientific challenges into opportunities that drive or sustain the development of your innovations.
â„“ Pharmaceuticals â„“ Medical Devices â„“
Why choose
ORPHAN QUANTUM?
CROSS-FUNCTIONAL
EXPERTISE
A broad experience covering both pharmaceuticals and medical devices, from preclinical to post-market stages.
I contribute to integrated regulatory operations and strategies, combining compliance, agility, and proactive evaluation.
TRUSTED-BASED
PARTNERSHIP
As an independent consultant, ORPHAN QUANTUM is above all a human and strategic partnership.
I engage deeply in your projects to build a collaboration founded on transparency, trust, and long-term value creation.
RESPONSIVENESS
AND FLEXIBILITY
My flexible model allows me to adapt quickly to your specific needs.
I help you design pragmatic, compliant, and immediately actionable solutions for your ongoing regulatory, clinical, and scientific activities.
YOUR SUCCESS,
MY PRIORITY
My mission is to accelerate and secure the development of your therapeutic innovations.
I am committed to ensuring their regulatory compliance and helping you enhance their scientific and medical value, contributing to their commercial and therapeutic success
DISCOVER ORPHAN QUANTUM
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Step into the world of ORPHAN QUANTUM and discover how my approach can strengthen your innovative projects.
From concept to regulatory compliance, from preclinical to clinical development, I support you at every stage, integrating strategy, excellence, and an international vision.
“My ambition is to combine scientific rigor, regulatory integrity, and strategic vision to foster responsible and sustainable therapeutic innovations, through multidisciplinary collaboration with R&D stakeholders.
Each collaboration is an opportunity to give meaning to my work, to make a meaningful contribution to science and public health, while offering my support where it can be most impactful".








