Ensuring Compliance and Streamlining Market Access through Regulatory Expertise
Our regulatory services help navigate complex local and international requirements, ensuring your healthcare products reach the market efficiently and in full compliance.
Comprehensive Regulatory Solutions for Healthcare Products
Monitoring Force provides expert regulatory services designed to guide your product through the approval process. We ensure compliance with local and international regulations, while providing strategic support to streamline submissions and optimize market access in the healthcare industry.
01
Regulatory Strategy Development
We create tailored regulatory strategies based on the unique requirements of each market. Our experts analyze local and international regulations, ensuring that your product complies with all necessary standards to accelerate approval and minimize roadblocks.
02
Dossier Preparation and Submission
Our team manages the preparation and submission of regulatory dossiers, ensuring that all necessary documents are complete and accurate. We work closely with regulatory authorities to streamline the submission process and reduce delays in getting your product to market.
03
Compliance with Local and International Regulations
We provide guidance on navigating the ever-evolving regulatory landscapes, including local regulations in the Gulf region and international standards like ICH and FDA guidelines. This ensures your product adheres to the necessary compliance requirements throughout its lifecycle.
04
Post-Market Regulatory Support
After product approval, we offer continued support with post-market surveillance, regulatory updates, and safety reporting. We help maintain compliance with ongoing regulations, ensuring that your product remains on the market without interruption.
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 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 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
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.
Product development is a complex process requiring a deep understanding of regulations, safety requirements, product efficacy, and market preferences. Proper advice can help navigate these complexities, reduce risks of failure, accelerate time to market, and optimize product success.
Our Regulatory Market Access and Market Study service involves a detailed analysis of the regulatory landscape and an in-depth study of the GCC region’s market. We identify potential opportunities and barriers to market entry, allowing us to develop strategic market access plans tailored to your product.
Our Early Access Program is designed to expedite the introduction of your product into the GCC market. We manage all aspects of the process, including regulatory negotiation, risk management, supply chain logistics, and post-approval activities. This allows your product to reach users who need it most as quickly as possible, while ensuring the highest levels of safety and efficacy.