Address
304 North Cardinal St.
Dorchester Center, MA 02124
Work Hours
Monday to Friday: 7AM - 7PM
Weekend: 10AM - 5PM
Robust Statistical Methodologies for Reliable Results
We offer a comprehensive range of statistical services to meet the specific needs of each clinical study. From methodological design to data analysis and detailed reporting, we ensure accurate and actionable results.
We design robust statistical frameworks to guide the entire analysis process. Our services include calculating the appropriate sample size to ensure study power and validity, as well as preparing comprehensive documentation detailing the analysis and data processing methods.
Our methodologies are tailored to the specific needs of each study, ensuring a solid foundation for reliable and scientifically valid results.
We create randomization lists and simulated reports for clinical trial execution. Using advanced software tools like SAS and WPS, we perform precise statistical analyses and provide secure access through web-based solutions for data management.
Our services also include statistical programming and management of Data Clarification Forms (DCFs) to ensure data integrity throughout the analysis process.
We provide detailed statistical reports, including tables, figures, and in-depth interpretations of the results. We use MedDRA dictionaries for adverse events and Whodrugs for concomitant treatments, ensuring consistent and accurate data classification.
Our reports are designed to provide a clear and comprehensive view of study results, facilitating informed decision-making and the publication of findings.
Our team of statistical experts has extensive experience and in-depth knowledge of advanced methodologies. We ensure that all analyses are performed according to rigorous standards and validated to guarantee reliable results.
We develop study-specific statistical methodologies, including the design of statistical analysis plans and the determination of appropriate sample sizes. We ensure that each study is designed to maximize statistical power and result validity, in close collaboration with research teams.
We use advanced software tools such as SAS and WPS for programming and executing statistical analyses. Our experts ensure precise analyses that comply with protocols, delivering reliable and reproducible results. Rigorous quality checks are performed at every stage to maintain data integrity.
We create clear and informative data visualizations, including charts, tables, and figures, to facilitate the interpretation of results. Our detailed reports provide in-depth interpretations to support informed decision-making, highlighting key trends and conclusions.
We write comprehensive and accurate scientific reports, tailored to academic journal standards and regulatory requirements.
Our experts create visually engaging and scientifically rigorous presentations, perfect for conferences or strategic meetings.
Abstract, Article, and Poster Writing and Submission
We operate across numerous therapeutic areas to provide healthcare solutions tailored to diverse needs.
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.
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.
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, 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, 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.
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.
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.
Explore the key metrics that showcase our continuous growth, expertise, and global impact.
Whether it’s clinical research, data management, or scientific consulting, Monitoring Force Group is here to help you achieve your goals.