Interventional Studies from Phase Ib to IV
From early-stage trials to post-market studies, we ensure your healthcare products are safe, effective, and compliant with global standards.
Comprehensive Management of Interventional Studies
Monitoring Force offers complete management of interventional studies from Phase Ib to IV. Whether it’s early-stage safety assessments or large-scale efficacy trials, we ensure that every phase of your study adheres to international standards and local regulations. Our expert team manages every aspect of clinical trials, from protocol design to the final report, ensuring that your product advances smoothly through the clinical development process.
01
Phase Ib and II
We specialize in conducting early-phase trials that focus on optimizing dosage and assessing safety and initial efficacy. Our expert team works closely with you to design precise study protocols and manage the trial efficiently, ensuring compliance with international standards while addressing local regulations and specific healthcare challenges.
02
Phase III
These large-scale trials aim to confirm your product’s efficacy and monitor adverse reactions in diverse populations. We provide end-to-end management, from regulatory submissions to data monitoring, ensuring every aspect of the study is executed smoothly and delivers reliable, compliant results to support your product’s market approval.
03
Phase IV
Post-marketing studies are crucial for assessing the long-term safety and effectiveness of your product in real-world conditions. Our team ensures ongoing support for collecting robust data, addressing regulatory requirements, and providing insights that enhance your product’s continued success in the healthcare market.
Tailored Protocols and Real-World Data Collection
Monitoring Force creates customized protocols for Non-Interventional Studies, ensuring rigorous real-world data collection. We guarantee regulatory compliance while delivering reliable and in-depth analyses to support your decision-making.
Study Design
We develop customized NIS protocols that align with your goals while respecting ethical and regulatory standards. Our approach ensures real-world data collection without disrupting routine medical practices, providing actionable insights into product performance.
Regulatory Approvals
We expertly navigate complex regulatory landscapes for non-interventional studies. From submission to approval, we manage the entire process to ensure compliance with local and international guidelines, minimizing delays and facilitating smooth study launches.
Data Collection & Monitoring
Using advanced tools, we ensure precise real-world data collection. Continuous site monitoring guarantees that all data adheres to study protocols and regulatory standards, delivering reliable and compliant results throughout the study.
Statistical Analysis
Our expert statisticians provide robust analysis of real-world data, extracting key insights to inform healthcare decisions. These analyses support regulatory submissions and market access strategies, validating your product’s long-term safety and effectiveness.
Why Choose Us ?
When it comes to Clinical Research & Management, Monitoring Force stands out for several reasons
Proven Expertise
With over 20 years of experience serving the European and the North African market, we have a deep understanding of the complexities and challenges of clinical research. We bring this expertise to the GCC region, ready to help you navigate the unique landscape of healthcare here.
Patient-Centered Approach
We believe in putting patients at the heart of everything we do. Our services are designed to benefit patients, from providing early access to new treatments to empowering patients with knowledge about their condition and treatment options.
Comprehensive Services
From the conception and management of clinical and Real Word Evidence studies to early access programs and patient education, we offer a comprehensive suite of services. This means you can manage all your clinical research needs in one place, with one trusted partner.
Commitment to Ethical Research and Authorities requests
We are committed to conducting research that is ethical, responsible, and beneficial to patients. We adhere to strict ethical guidelines in all our services, ensuring the safety and well-being of patients involved in our studies.
Partnerships for authentic experiences.
Building Collaborative Relationships for Genuine Impact
Monitoring Force Gulf is not just a service provider – we are a partner in your journey towards healthcare advancement. We believe in the power of collaboration to create authentic and impactful experiences in clinical research and management. With over 20 years of experience in Europe, in North Africa and a deep understanding of the GCC healthcare landscape, we bring a unique blend of global insights and local relevance to our partnerships. We work closely with you, understanding your specific needs and goals, to deliver services that truly resonate with your project objectives and the communities you serve. Choose Monitoring Force as your partner for genuine, impactful experiences in the GCC region and beyond.
Team Of Experts
Dr. Amin Kadi
President, Monitoring Force
With over 30 years of combined experience in cardiology and CRO activities, Dr. Amin Kadi epitomizes the blend of medical expertise and industry leadership, driving innovations and excellence at the forefront of healthcare research.
Samy Aloulou
General Manager, Monitoring Force Gulf
brings 15 years of seasoned experience in business and operational development. His strategic vision and leadership have been pivotal in the growth and success of Monitoring Force Gulf, setting new standards in the industry.
Baptiste
Project Director
With a decade of project management in the CRO sphere, Baptiste is known for his meticulous approach and results-driven leadership. His expertise in steering complex projects has been instrumental in delivering exceptional outcomes for our clients.
Frequently Asked Questions
Have questions about our services? Check out our FAQ section to find answers to common questions. If you don’t find what you’re looking for, don’t hesitate to get in touch – we’re here to help.
Our Clinical Research & Management service includes Clinical and Real-World Evidence Study Conception & Management, Early Access Program, and Patient Education Program. We offer a comprehensive suite of services designed to support you at every stage of your clinical research journey.
At Monitoring Force Gulf, we are committed to maintaining the highest standards of quality in all our services. We have a team of experienced professionals who bring their expertise to every project. We also follow strict ethical guidelines and adhere to all relevant regulations to ensure the safety and success of your research.
At Monitoring Force Gulf, we take great pride in the success of our customers. A significant majority of our customers have achieved their goals with our tailored solutions and dedicated support. Our expertise and collaborative approach empower our clients to navigate the challenges of clinical research and management effectively, resulting in successful outcomes.
ou can contact us through the “Contact Us” page on our website. We would be happy to discuss your service needs and how we can support your healthcare project in the GCC region and beyond.