Conducting Interventional Studies

Expert management of your clinical trials, from Phase Ib to Phase IV.

Study Design and Planning

We begin each interventional study with a thorough analysis of strategic, scientific, regulatory, timeline, and budgetary objectives before establishing a detailed and rigorous plan. Our teams design tailored protocols aligned with strategic goals while ensuring strict compliance with local and international regulations.

Protocol Development
Sample Size Calculation and Randomization
Regulatory Submission and Compliance

We develop precise clinical protocols tailored to the specific needs of each study. Designed to ensure patient safety and scientific validity, our protocols also meet regulatory requirements, providing a solid foundation for every clinical study.

Optimized sample size calculation and randomization to achieve representative and reliable results.

We manage the entire regulatory submission process, from dossier preparation to obtaining the necessary approvals. Our expertise in local and international regulations streamlines the approval process, ensuring compliance at every step.

Operational Management and Monitoring

Effective operational management is essential for the success of your clinical trials. We coordinate all stakeholders and ensure continuous monitoring to guarantee data quality and participant safety.

Investigator Coordination

Selection of experienced investigators and sites, ensuring they have the patient pool and resources necessary to successfully execute assigned protocols while meeting quantitative, qualitative, and timeline objectives.

Monitoring with 100% Source Data Verification

Rigorous trial monitoring to ensure compliance with protocols and participant safety, with continuous responsiveness.

Pharmacovigilance Management

Rigorous safety monitoring to ensure participant safety and compliance with regulatory standards.

Results Analysis and Study Closure

Final Data Collection

Monitoring, collection, and validation of final data, ensuring its quality and completeness.

Advanced Statistical Analysis

Using advanced statistical methods and tools to analyze study results.

Report Writing and Submission

Preparation of study reports compliant with scientific and regulatory requirements, ready for submission to the competent authorities.

Results Presentation

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

Therapeutic Areas

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

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.

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.

Our Latest Publications

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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 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.

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