Hello, I am Meriem Bouslouk-Marx

the Founder of MBM Future Health

I advise international stakeholders on access to novel medicines. Public Health and evidence-based decision-making have been the centre of my work for 20 years, almost 10 years at Germany’s top health policy body, the G-BA.

 

DISCOVER MY SHORT BIO:
Health Authority in Germany

When the German Federal Government introduced AMNOG – the legislation on the benefit assessment of medicinal products in 2011, I joined the initial small team at the Federal Joint Committee G‑BA in charge of implementing the procedure. In this position, I prepared binding Decisions published in the Federal Gazette in Germany. My main responsibilities included conducting Scientific Consultations with pharmaceutical companies and involved Regulatory Authorities on clinical trial design. Moreover, I joined the initial grant allocation team at the Innovation Committee when the German Federal Government created an Innovation Fund with an annual budget of €300 million to improve the quality of medical care.

Rare Diseases

From the outset, my particular focus at the Federal Health Authority in Germany was on rare diseases. The German Government had introduced incentives for the national Health Technology Assessment (HTA) of rare disease therapies, commonly called orphan drugs. I coordinated the new national HTA procedure of orphan drugs in Germany. Besides medical and statistical expertise, this specific procedure required targeted health policy considerations. The launch of gene therapies in Germany even increased the challenges in this field.

International Career

After my French Baccalauréat at the Lycée Descartes in Rabat, Morocco, I graduated with a PhD in Dental Medicine from the Friedrich Schiller University in Jena, Germany. In connection with my postgraduate Master of Science in International Health from the Charité University Hospital in Berlin, I managed Public Health projects in Africa, especially in Tanzania (Amref Health Africa and rural health), Morocco (WHO Country Office), Burundi and Guinea (Health Focus GmbH). From the start at the German Health Authority in 2011, I was entrusted to promote the G-BA’s work outside Germany: In lectures and speeches, within and outside the G BA, I fostered partnerships with European and international organisations. I speak French, Arabic, German and English.

Dr. Meriem Bouslouk-Marx, Founder of MBM Future Health

‘Combining integrity and enthusiasm induces the best value.’

Equipped with my experience, I have been supporting my clients worldwide for several years with my company MBM Future Health.

Relevant publications

Expert Opinion

G-BA benefit assessment of new orphan drugs in Germany

My experience at the Federal Joint Committee G-BA with the benefit assessment of orphan drugs in Germany under AMNOG. Facts on policy and scientific procedure.

Pharmaceutical Executive

Efficacy Controversy Hits European COVID-19 Vaccine Rollout

Donald Macarthur and I discuss post-approval findings of national committees in Europe for the use of a new COVID-19 vaccine in their populations.

Tagesspiegel Background

Mit der EMA auf der Überholspur/With EMA on the fast track

I take a stance on the political decisions and procedures for approval and distribution of vaccines in Germany and in the EU, also in the light of public criticism.

In action

Lecturer and Speaker at the Market Access Society (MAS). MORE INFORMATION

Adviser at Project HERCULES, a Duchenne UK Global Collaboration. MORE INFORMATION

Speaker at the Brazilian Health Regulatory Agency Anvisa. GENE AND ADVANCED THERAPIES: Creating Value in the Patient Journey and the Health System. MORE INFORMATION

Adviser with the Alliance for Regenerative Medicine (ARM). Getting Ready: Recommendations for Timely Access to Advanced Therapy Medicinal Products (ATMPs) in Europe. MORE INFORMATION

In references

AMED, Japan Agency for Medical Research and Development (2020) Development Trend Survey of Ultra Orphan Drugs. MORE INFORMATION

Schoonveld, E. (2020). The Price of Global Health: Drug Pricing Strategies to Balance Patient Access and the Funding of Innovation (3rd ed.). Routledge. MORE INFORMATION

European Commission (2019) Study to Support the Evaluation of the EU Orphan Regulation.  MORE INFORMATION

OECD, Organisation for Economic Co-operation and Development (2018) Pharmaceutical Reimbursement and Pricing in Germany. MORE INFORMATION

Recent News

Access to Gene Therapies

Access to gene therapies has changed the healthcare landscape. Gene therapies are a field of study for researchers and, at the same time, a...

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