TARGET SECTORS

TARGET SECTORS ℓ

CROSS-FUNCTIONAL EXPERTISE SERVING YOUR SUCCESS.

IN THE WORLD OF HEALTH RESEARCH AND INNOVATION, EVERY SECTOR HAS ITS SPECIFICITIES, CHALLENGES, AND OPPORTUNITIES.

With cross-disciplinary expertise and an adaptive approach, ORPHAN QUANTUM positions itself to deliver specialized services covering every stage of the R&D process for drugs and medical devices, from preclinical research to post-marketing compliance.

Whatever your field, my commitment is to provide tailored support to guide, enhance, and accelerate your projects.

Explore my target sectors and discover how I can bring value to your organization.

Accelerate your development

and strengthen your global compliance.

I provide full regulatory lifecycle management support, including CMC strategy, variations, post-market activities, and global submissions to ensure the quality, continuity, and compliance of your products worldwide.

PHARMACEUTICALS

COMPANIES

Expand your missions with

complementary regulatory and clinical expertise.

With my support, enhance your consulting services through a cross-functional scientific and regulatory perspective tailored to the pharmaceutical sector’s strategic and operational needs.

CONSULTING FIRMS
IN STRATEGY

Maximize the impact

of your international collaborations.

I help structure Horizon Europe or similar collaborative projects with a holistic vision that integrates compliance, development strategy, and EU regulatory alignment.

EUROPEAN PROJECT

CONSORTIUMS

Strengthen your projects with transversal

regulatory and documentation expertise.

Rely on my support for GCP compliance, clinical documentation drafting and review, and regulatory coordination throughout your clinical trials.

CLINICAL RESEARCH

ORGANIZATIONS

Accelerate your research and secure

your scientific and regulatory activities.

I support your preclinical-to-clinical transition, ensuring scientific rigor, ethical integrity, and regulatory compliance from the early design of your studies.

HOSPITALS
AND RESEARCH INSTITUTES

Enhance your publications

with rigor and scientific clarity.

I assist in strengthening the editorial quality and technical precision of your scientific articles and specialized communications, ensuring accuracy and credibility.

SCIENTIFIC
JOURNALS

Build solid regulatory foundations

for your innovation.

I help you design development strategies, anticipate CMC and clinical requirements, and structure your first registration dossiers, establishing a compliant and scalable growth pathway.

BIOTECH
START-UPS

Turn research

into compliant, high-value innovation.

With my support, secure the regulatory compliance of your technologies and optimize their transfer to industry, maximizing both scientific impact and economic value.

TECHNOLOGY TRANSFER
OFFICES

Amplify the impact of your public health initiatives.

I translate scientific and regulatory issues into clear, accessible language to educate patients, inform the public, and support your advocacy and educational programs.

NON-PROFIT

ORGANIZATIONS