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Regulatory affairs and market access for pharmaceutical and biotech companies in France

About APC

Access Pharma Consulting – Pharmaceutical Market Access and Regulatory Strategy in France

​About Access Pharma Consulting

Market Access & Regulatory Strategy for France

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Access Pharma Consulting is a France-based market access and regulatory consulting firm supporting pharmaceutical, biotech, medical device, and medical cannabis companies entering or expanding in the French market.

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We provide senior-level regulatory strategy, market access planning, pricing and reimbursement expertise, and stakeholder engagement support aligned with ANSM and HAS requirements.

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Our consultancy supports international healthcare companies across specialty and hospital-driven markets, addressing complex French regulatory pathways and access challenges.

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With over 10 years of pharmaceutical industry leadership, Access Pharma Consulting combines medical expertise, regulatory intelligence, and commercial strategy to accelerate successful market entry in France.

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We work directly with executive teams to design decision-ready, locally grounded, and globally aligned go-to-market strategies for France.

More than navigating the French healthcare system, we unlock it.

Strategic Market Access &
Regulatory Services 

Tailored Expertise Across the Pharmaceutical & Biotech Product Journey

At APC, we design and deliver high-level market access and regulatory strategies tailored to your product, development stage, and market objectives.

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Whether you're exploring the French market, preparing a launch, or refining your access strategy, we align medical, regulatory, and commercial dimensions to unlock success.

Why Choose Access Pharma Consulting for Market Access ?

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Led by Dr. Dounia Farajallah, PharmD & ESSEC-trained strategist, with a strong pharmaceutical industry background, combining medical insight with executive-level business and market access expertise.

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More than 12 years of experience in the pharmaceutical industry, including leadership roles across international environments and hands-on involvement in the launch and management of a French subsidiary for a global pharma group.

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Proven experience in regulatory approvals, market access strategy, and pricing negotiations across complex therapeutic areas.

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Deep mastery of the French healthcare system, including ANSM and HAS interactions, reimbursement pathways, and hospital tenders.

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Acting as a single senior interface to accelerate decision-making, reduce regulatory risk, and avoid costly misalignment between medical, regulatory and commercial teams across complex products and markets.

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