Clinical Study Design and Management

Optimize Your Clinical Projects with Our Expertise and Integrated Management

We Cover Every Step

Our expertise spans Phase Ib to IV trials and includes a wide range of non-interventional studies, such as registries, post-authorization safety studies (PASS), and post-marketing surveillance (PMS) studies.

Clinical Study Design
Project Management
Risk Management

Rigorous Planning: We develop detailed clinical research plans and tailored protocols for each project, ensuring that every aspect of the study is meticulously designed to meet the client’s specific objectives.

Protocol Development: We design clear and detailed protocols tailored to the specific needs of each study.

Objective Setting: We clearly define study objectives to ensure relevant and actionable results.

Global Coordination: Our project management team ensures seamless integration of every study phase, enabling efficient execution and timely delivery.

Ongoing Supervision: We oversee all study phases, from design to final data analysis, ensuring flawless management throughout.

Regular Updates: We maintain proactive and consistent communication with all stakeholders to ensure transparency and engagement throughout the project.

Proactive Identification: Through our proactive approach, we identify and mitigate potential risks early in the project, ensuring study continuity and success.

Strategic Solutions: We implement strategic solutions to address identified risks and minimize their impact on the project.

Continuous Monitoring: We constantly monitor the study’s progress to detect and manage emerging risks effectively.

Project Management and Coordination

Our project managers develop detailed plans to ensure smooth execution and timely delivery. We believe in transparent coordination, seamlessly integrating each phase of the clinical study. Through proactive communication, we keep all stakeholders informed and engaged throughout the process.

Planning and Execution

We create detailed project plans tailored to your specific objectives, ensuring efficient execution and timely delivery.

Global Coordination

Each phase of the study is meticulously coordinated to ensure seamless integration, from initial design to final analysis.

Communication Management

Our proactive communication approach ensures that all stakeholders receive regular updates and remain engaged throughout the project.

Strategic Selection of Sites and Investigators

Investigator Selection

We select investigators with recognized clinical expertise and solid research experience, ensuring the generation of high-quality data.

Site Feasibility Studies

Detailed feasibility studies enable us to evaluate site recruitment capabilities and performance, ensuring optimal selection.

Site Viability

Selected sites must meet strict criteria for patient population, technology, and logistics, ensuring seamless study execution.

Mastering Regulatory Compliance

Navigating the complex regulatory landscape is essential for the success of any clinical study. We handle regulatory submissions and approvals, ensuring full compliance and adherence to timelines.

Strategic Planning

Development of region-specific and study-specific strategic plans, ensuring efficient progress through regulatory milestones.

Regulatory Submissions

Management of all submission stages, from initial documentation to final approval.

Continuous Support

Providing ongoing support to address regulatory inquiries and ensure uninterrupted compliance throughout the study.

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.