Address
304 North Cardinal St.
Dorchester Center, MA 02124
Work Hours
Monday to Friday: 7AM - 7PM
Weekend: 10AM - 5PM
A Strategic Partner for Every Step of Your Clinical Development
Integrated services to ensure quality, compliance, and innovation in your healthcare projects
Our Services
We provide end-to-end support for the development of your healthcare products. From concept to delivery, every stage is managed to ensure quality, compliance with international standards, and on-time results.
Interventional Studies IB–IV
Comprehensive management from study design and implementation to the delivery of final reports, with rigorous planning and efficient execution to ensure high-quality and relevant results within the agreed 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 Support Programs (PSP)
Integrating patient needs through dedicated, patient-centered programs that provide continuous support and actively engage them throughout their care journey.
Regulatory Affairs
Submission and approval of study authorization files for all types of health products, in full compliance with current regulations in France, Europe, and worldwide. We ensure regulatory compliance of your products and closely monitor regulatory developments.
Biometrics
Clinical data management and statistical analysis covering all key steps, including data entry, verification, validation, reconciliation, and advanced statistical analyses to ensure reliable results.
Market Access
Our market access services help you navigate the complexities of local and international regulations, ensuring the efficient and compliant launch of your products.
Advisory, Writing, and Publication
We provide consulting and scientific writing services for publications, including literature reviews, abstract drafting, poster and article preparation, as well as the development of presentation materials for your study results.
Scientific Board Setup and Management
We support the establishment, administrative and financial management, content preparation, and facilitation of scientific boards, ensuring the scientific and strategic relevance of your projects.
Training
Specialized programs in clinical research, pharmacovigilance, medical writing, and regulatory affairs. Each training is designed to address specific needs, ensuring a thorough understanding of current practices and strict compliance with applicable standards.
Therapeutic Areas
We operate across a wide range of therapeutic areas to provide healthcare solutions tailored to diverse needs.
Our Clients
20 Years of Growth and Innovation
For 20 years, Monitoring Force Group has been dedicated to innovation and continuous development in the field of clinical research. Our subsidiaries, strong partnerships, and diverse expertise enable us to effectively address the evolving needs of the healthcare industry.
