We provide scientific support to advance clinical research through data development, analysis, and innovation.
Your Journey with Us
Awarded the 2025 Best Healthcare Entrepreneurial Initiative by King Saud bin Abdulaziz University for Health Sciences.
We participated in the 16th Saudi Society of Dermatology and Dermatologic Surgery with a real-world study on cutaneous adverse reactions.
We proudly participated as an exhibitor at the Global Health Exhibition, one of the region’s premier healthcare events.
Clinical Research
End-to-end clinical research services designed to generate high-quality, regulatory-ready data. From study design to data analysis and final reporting, every phase is executed with scientific rigor and compliance to global standards, ensuring reliable results that support regulatory approval and market success.
Evidence Development
We create credible and clinically relevant evidence that supports your project at every stage. Our comprehensive services include real-world evidence, high-quality biostatistics, meta-analyses, and systematic reviews, all designed to provide a strong, evidence-based foundation. With a focus on scientific integrity and regulatory compliance, we deliver evidence that meets the highest standards to promote informed decision-making and successful market positioning.
Research & Development
Innovative R&D services designed to drive scientific advancement and product development. Our offerings include molecular modeling, preclinical study planning, and pilot studies, providing a solid foundation for your product’s success. With a focus on robust methodologies and evidence-based research, we help accelerate your R&D process, guiding your product through IND submissions and positioning it for successful clinical trials and market introduction.
Regulatory Affairs
Strategic support to navigate complex regulatory pathways and maintain compliance with local and global standards, including IRB and ethics committee approvals. Our team offers expert guidance on regulatory submissions, approvals, and ongoing compliance, helping you meet the requirements of regional and global regulatory bodies.
Medical Affairs & Communication
Comprehensive support that bridges the gap between clinical research and practice. Our medical affairs services include scientific communication, data dissemination, patient engagement, and medical strategy development to for effective positioning. We provide healthcare professionals and regulatory bodies with data-driven and accurate information that promotes informed decision-making and product adoption.
We support clients from various sectors with high-quality evidence that drives impactful decisions and advances their projects forward. Our offerings are designed to support healthcare professionals, organizations, and companies in making informed, evidence-based decisions. Our team brings knowledge and expertise in clinical research, regulatory affairs, data analysis, project management, and scientific consulting to every project so that we deliver tailored solutions to meet your specific needs.
2
Plan
Develop a tailored project roadmap with clear objectives and deliverables.
1
Consult
Discuss your goals and explore how we can support your needs.
3
Execute
Implement the plan with precision, accuracy, and scientific rigor.
4
Deliver
Deliver results that are impactful, and ready for implementation.
Why Maxeome?
Maxeome is a strategic Clinical Research Organization built for today’s healthcare landscape. We combine scientific rigor with commercial insight to help companies make smarter, faster, and more evidence-driven decisions.
We’re not just here to execute, we’re here to think with you. We deliver strategy backed by evidence.
From protocol design to market impact, we align clinical strategy with wider business goals.
Our integrated approach supports every stage of the product’s lifecycle to ensure that the research you invest in delivers value beyond publication.
Evidence-First Mindset
We design and execute research that answers real clinical and regulatory questions to improve patient outcomes.
Strategic from Day One
Every project is designed with your endgame in mind. Whether that’s regulatory approval, market access, or practitioner adoption. We connect research to real-world impact.
Clinically Grounded & Business Aligned
Our studies are scientifically rigorous and commercially relevant. We focus on evidence that matters — to regulators, clinicians, and the market.
Agile, Expert-Driven Team
We operate lean, with expert consultants driving every step. That means fewer handoffs, faster timelines, and a direct line to strategic thinking.