MY SERVICES
Regulatory Strategy.
Clinical Development.
Data Engineering.
Scientific Expertise.
Compliance.
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Discover my integrated approach to supporting you in the landscape of healthcare R&D.
MY SERVICES â„“
HOW CAN I HELP YOU ?
NAVIGATING THE WORLD OF DRUG AND MEDICAL DEVICE R&D REQUIRES A DEEP UNDERSTANDING OF REGULATORY, CLINICAL, AND SCIENTIFIC CHALLENGES.
With solid experience in global regulatory affairs, clinical development, and scientific strategy, I help you build, align, and enhance your therapeutic innovations.
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My approach is based on a holistic vision of product development, with services designed to support you at every phase — from preclinical to post-market — while mastering the interactions between science, quality, regulation, and strategy.
By integrating ORPHAN QUANTUM into your operations, you gain a partner capable of anticipating authority expectations, optimizing R&D processes, and ensuring scientific and regulatory coherence across all stages of your project.
Discover my services and how I can help you move your projects forward.
" Helping you make informed scientific and regulatory decisions, from preclinical through post-market phases, with both strategic insight and operational execution ".
STRATEGIC R&D
SUPPORT
" Structuring and analyzing scientific, medical, and regulatory data to prepare strong dossiers, reports, literature reviews, or state-of-the-art analyses ".
DATA ENGINEERING
RESEARCH & ANALYSIS
" Comprehensive management of R&D, clinical, and regulatory projects.
Coordination, planning, and reporting to ensure efficiency and on-time delivery ".
PROJET
MANAGEMENT
" Creating clear, impactful materials to highlight your scientific innovations, boost visibility, and support your commercial strategy ".
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MARKETING
COMMUNICATION
" Drafting and reviewing CTD, MAAs, variations, clinical documents, protocols, and scientific publications - transforming complex data into clear and compelling communication ".
SCIENTIFIC AND REGULATORY
WRITING
"Sharing knowledge in R&D, regulatory affairs, and project management to strengthen your teams’ internal capabilities and streamline project execution ".
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TRAINING
AND WORKSHOPS
" Managing submissions and interactions with health authorities across Europe, Asia, and the Middle East to secure market access and maintain compliance ".
REGULATORY
OPERATION
REGULATORY
STRATEGY
“Need to structure your regulatory processes and submissions?
Together, we can define a strategy suited to your development stage, technical constraints, and market ambitions. My goal: ensure your dossiers align with authority expectations to accelerate compliance and market access.”​
My consulting, writing, and regulatory support services help you prepare, draft, and manage your submissions while facilitating efficient interactions with health authorities
MARKETING
POSITIONNING
"Developing a molecule or technology and looking to showcase its potential?
I help you define the best therapeutic and regulatory positioning, analyze competitors, and identify differentiating levers to maximize both medical and commercial value."
My data engineering, communication, and consulting services can support your market studies, positioning analysis, and product valorization​
CLINICAL
STRATEGY
"Starting or consolidating a clinical development program?
I support you in designing and optimizing clinical development plans and drafting key documents and reports, tailored to your innovation and compliant with GCP standards."
My consulting, project management, writing, and regulatory support services help you obtain approvals to initiate clinical trials or leverage your study results effectively.
COMMUNICATION
STRATEGY
"Want to increase the visibility of your healthcare R&D work?
Count on me to deliver credible, clear scientific communication tailored to your audience - researchers, clinicians, partners, or investors".
My writing, communication, data engineering, and training services can be leveraged to create high-impact materials, publications, and presentations aligned with your visibility and dissemination goals.
SCIENTIFIC
STRATEGY
"Looking to turn your research into tangible therapeutic innovations?
I help you structure R&D programs, harmonize preclinical and clinical plans, and strengthen the scientific and medical consistency of your projects from the earliest phases."
My consulting, project management, writing, and data engineering services help you design solid preclinical and clinical development plans and ensure scientific and regulatory robustness from the start.
Discover the deliverables that my cross-functional profile can offer you.
CHOOSE THE PLAN
THAT FITS YOU
I adapt my approach
to your needs.
CONTINUOUS SUPPORT
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Guaranteed availability.
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Step-by-step assistance throughout your projects
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Spread out your expenses.
ON-DEMAND SUPPORT
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Mobilization according to your needs.
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Quick response to your specific needs.
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Cost proportional to time spent.
EXPLORE THE DIVERSITY OF SECTORS TO WICH MY SERVICES CAN BE ADAPTED
Do you belong to the private sector ?
Or are you a member of the academic world ?
Depending on your structure, your projects require a tailor-made approach.
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My cross-functional services can be adapted to your ambitions and needs to help you achieve your objectives.
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From fondamental research to clinical development, I'm here to help you turn your challenges into opportunities.
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“My services aim to combine my passion for science with my commitment to ethics and rigor, collaborating in a multidisciplinary manner with R&D stakeholders to meet stimulating challenges.
Each project is an opportunity to give meaning to my work, to make a significant contribution, and to bring real added value to public health."
DISCOVER MY PROFESSIONAL PROFILE AND VALUES
