Strategic Support for Healthcare Products

Expert guidance tailored to every phase of your project.

Our Services

We provide a comprehensive range of services to support the development of your healthcare products. Every step of the process is covered to ensure reliable results that meet international standards, all while respecting your timelines.

Interventional Studies 1B-IV

Comprehensive management from study design and implementation to the delivery of your clinical study report. We ensure rigorous planning and efficient execution to deliver high-quality, relevant results within the defined timelines.

Non-Interventional Studies

Our non-interventional studies provide valuable insights into the real-world use of drugs and medical devices, ensuring a deeper understanding of their effectiveness and safety.

Patient Centricity Program (PSP)

Integrating patient needs through tailored programs that provide continuous support and actively engage them in their care journey.

Regulatory Affairs

Submission and approval of authorization dossiers for all types of studies across all categories of healthcare products, in full compliance with regulations in France, Europe, and worldwide. We ensure regulatory compliance for your products and monitor regulatory updates closely.

Biometrics

Clinical data management and statistical analysis encompass several key steps, including data entry, verification, validation, data reconciliation, and in-depth statistical analyses to ensure reliable results.

Acces Market

Our market access services help you navigate the complexities of local and international regulations, ensuring the efficient and compliant launch of your products.

Consulting, Writing, and Publication

We provide consulting and writing services for scientific publications, including literature searches, abstract writing, poster and article preparation, as well as support for presenting your results effectively.

Establishment and Management of Scientific Boards

We assist in the establishment, administrative and financial management, preparation of scientific content, and facilitation of scientific boards to enhance the scientific and strategic relevance of your projects.

Training

Specialized programs in clinical research, pharmacovigilance, medical writing, and regulatory affairs. Each training is tailored to meet specific needs, providing in-depth understanding of current practices and ensuring strict compliance with applicable standards.

20 Years of Growth and Innovation

For 20 years, Monitoring Force Group has been committed to innovation and continuous development in the field of clinical research. Our subsidiaries, strong partnerships, and diverse expertise enable us to effectively meet the evolving needs of the healthcare products industry.

Over 300 Completed Projects

24 Therapeutic Areas

75+ Clients and Partners

100+ Publications

Our Clients

Why Choose Monitoring Force Group?

In a constantly evolving healthcare landscape, choosing the right partner for your clinical research needs is crucial. At Monitoring Force Group, we understand the complexities of this field and bring the expertise, experience, and dedication necessary to support your success.

Global Experience, Local Expertise

With over 300 completed projects, we deliver tailored expertise for every project. Our team of professionals is highly experienced across a wide range of therapeutic areas.

Integrated Services

We provide a comprehensive range of services, from designing your development plans and conducting studies to data collection and analysis. We ensure consistent quality at every step of the process.

Constant Innovation

We invest in the latest technologies and methodologies to deliver high-quality results. Our innovative approach enables us to effectively address the evolving needs of clinical research.

A Trusted Partner

We are more than a CRO; we are a trusted partner. We work closely with our clients to understand their needs and exceed their expectations, ensuring the success of their projects.

Therapeutic Areas

We operate across numerous therapeutic areas to provide healthcare solutions tailored to diverse needs.

What Our Clients Say About Us

Nothing speaks more to our commitment, expertise, and impact than the words of our clients. These testimonials reflect the trust we’ve earned and the partnerships we’ve built. Discover why organizations worldwide choose Monitoring Force as their trusted partner in clinical research.

“Working with Monitoring Force has revolutionized our operations. Their expert guidance and practical solutions have helped us overcome complex scientific challenges with ease.”

Yahia El Mir,

CEO - Ziwig

“Working with Monitoring Force has been a game-changer for our clinical research initiatives. Their understanding of key challenges, innovative and pragmatic approach, and unwavering commitment have significantly enhanced our projects. They are not just a service provider but a true partner.”

Naimi Missoum;

Global Head of Medical Affairs NMD at Biogen

“Collaborating with Monitoring Force has been an exceptional experience. Their deep understanding of the healthcare landscape, combined with cutting-edge technology, has brought invaluable insights to our project. They truly stand out in their field.”

Jérôme Augustin,

CEO - NextKidney

“The expertise and professionalism of the Monitoring Force team were instrumental in the success of our recent clinical trials. Their attention to detail and proactive communication made the complex process smooth and seamless. They are a benchmark of excellence in healthcare research.”

Waleed Ghanima;

Professor at Østfold Hospital and the Institute of Clinical Medicine

Amin kadi - ceo

Amin Kadi, CEO of Monitoring Force Group and a cardiologist, has been leading the company since its inception over 20 years ago. Under his leadership, Monitoring Force has established a strong presence in Europe, the Middle East, and North Africa, delivering cutting-edge clinical and regulatory solutions across all healthcare products, always with a patient-centered approach.

Sophie Texier

Sophie Texier, Clinical Operations Director at Monitoring Force France, brings over 20 years of experience in clinical research. A strategic leader, she oversees international studies and ensures compliance with ICH/GCP standards, delivering high-quality results.

baptiste julliard

Baptiste Julliard, Project Director at Monitoring Force, is a cornerstone of the company with over 14 years of experience. A dedicated leader, he manages complex projects with precision and expertise, ensuring the success of clinical studies for nearly a decade.

Bernadette Darne

Dr. Bernadette Darné, Scientific and Medical Director at Monitoring Force, is a physician, epidemiologist, and statistician. With over 20 years of experience, she combines clinical and scientific expertise to lead complex projects and deliver high-quality results.

Samy Aloulou

Samy Aloulou, General Manager for the Gulf region, brings over 15 years of experience in business strategy implementation. His vision drives the development and growth of subsidiaries in the region.

Need help with your projects? Contact us today.

Expertise and Personalized Support

At Monitoring Force Group, we provide tailored support for every clinical research project. Our dedicated team ensures meticulous planning and efficient execution to deliver reliable and meaningful results.

Our Latest Publications

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Our Success Metrics

Explore the key metrics that showcase our continuous growth, expertise, and global impact.

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Transform Your Challenges with Us

Whether it’s clinical research, data management, or scientific consulting, Monitoring Force Group is here to help you achieve your goals.