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.
‘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...
Rare Diseases in Global Health
Rare Diseases Worldwide This year, People Living With a Rare Disease (PLWRD) have a chance to get the recognition they deserve in Global Health. To...
G-BA resolutions on afamelanotide for the rare disease erythropoietic protoporphyria RAPS EURO Convergence Europe in Berlin on 7 May 2024
Obstacles for patient access to medicines can happen at different stages of a medicine's life cycle. Therefore, marketing authorisation should not...