MY SERVICES
Scientific expertise.
Compliance
Regulatory strategy.
Clinical development
Data engineering.
Marketing insight.
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Discover my integrated approach to successfully navigating R&D landscape.
MY SERVICES â„“
HOW CAN I HELP YOU ?
NAVIGATING THE WORLD OF INNOVATIVE DRUG AND MEDICAL DEVICE RESEARCH AND DEVELOPMENT REQUIRES DEEP EXPERTISE AND A NUANCED UNDERSTANDING OF THE UNIQUE SCIENTIFIC AND REGULATORY CHALLENGES THIS SECTOR PRESENTS.
With a strong background in cross-functional scientific, regulatory, and medical affairs, my goal is to provide you with assistance and strategic, customized solutions for your drug and medical device development projects.
My services are designed to guide and support you at every step, turning obstacles into opportunities and ensuring that your innovations reach their full potential.
By integrating ORPHAN QUANTUM into your efforts, you will benefit from a dedicated partner who not only understands the complexities of healthcare R&D but also how to skillfully navigate through various phases to achieve tangible results.
Discover my services and how we can move your vision forward together.
"I help you make decisions and navigate the complex landscape of scientific, regulatory and marketing affairs with a strategic overview."
R&D STRATEGIC
CONSULTING
"Whether you need a study report, an article or a state-of-the-art report, I'll research, structure and analyze the scientific, medical, regulatory and socio-economic data you're interested in."
DATA ENGINEERING
RESEARCH & ANALYSIS
"I support you from the design to the implementation of your R&D projects with expert management for a smooth process."
PROJET
MANAGEMENT
“Use my marketing communication skills to ensure your message is recognized in the scientific community with clear, precise, and impactful digital tools to share, validate, and promote your discoveries.”
MARKETING COMMUNICATION
AND WEB DEVELOPMENT
"From scientific publications to regulatory submissions, benefit from my synthesis and writing skills to transform your complex data into clear communications that make a difference."
SCIENTIFIC AND REGULATORY
WRITING
"I offer customized training to enhance your knowledge of the processes of pharmaceutical and medical device R&D."
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TRAINING
AND WORKSHOPS
"Simplify your interactions with regulatory authorities by letting me manage the administrative aspects and follow-up of your processes."
REGULATORY
SUPPORT
MARKETING
POSITIONNING
"Do you have a molecule or a technology in development and want to assess its medical added value? Let me help you study and define the best therapeutic positioning to maximize its impact".
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My consulting and support, data engineering and training services are designed to help you unlock the potential of your innovations.
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REGULATORY
STRATEGY
"Do you need to structure your strategy? Together we can work out the best regulatory approach to accelerate and optimize your R&D and market access processes for your innovations"
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My consulting, writing and regulatory support services are designed to help you optimize your administrative procedures with the regulatory authorities.
SCIENTIFIC
STRATEGY
"Do you have the ambition to develop your discoveries into innovative new therapies or innovative devices ? Structure your preclinical R&D plan with a global vision and identify the essential points for a successful clinical transition by integrating me at your side."
My consulting and support, project management, writing and data engineering services are designed to help you to position a comprehensive R&D strategy from the earliest stages, ensuring a smooth transition from research to innovation.
COMMUNICATION
STRATEGY
"Would you like to share and promote your involvement in health R&D ? You can count on me to ensure transparent and impactful scientific communication to reinforce confidence in your data and your product".
My writing, data engineering, communication and training services are designed to help you share your discoveries in the research and innovation' ecosystem, with communication that both impacts and inspires.
CLINICAL
STRATEGY
"Each phase of clinical trials presents its own challenges. I can work with you to help ensure smooth progress, adapted to your innovations and in line with good clinical practice, ISO Standards and ICH guidelines".
My consulting, project management, writing and regulatory support services are designed to help you ensure a successful market launch with clinical expertise to guarantee regulatory conformity.
Discover the deliverables that my cross-functional profile can offer you.
CHOOSE THE PLAN
THAT SUITS YOU
I adapt my approach
to your needs.
LONG-TERM SUPPORT
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Guaranteed availability.
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Step-by-step assistance in 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.