Real World Data & Outcomes Research
Clinical Research & Real-World Evidence Made Simpler
A Look to the Future
We simplify evidence generation by connecting data to real outcomes, measurable results, and the impact of the product in practice.
More than just a research system, we offer an approach that generates continuous evidence over time. We monitor outcomes and responses under real-world conditions, with quality, regulatory compliance, and cost-effectiveness tailored to each project.
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Simplified Clinical Studies
Intelligent protocols, agile execution, cost proportional to your product.
We design and conduct simplified clinical studies, especially focused on nutraceuticals, herbal medicines, functional foods, and health products. Our focus is on generating robust clinical evidence with pragmatic protocols, efficient execution, and costs appropriate to the product's reality—without the unnecessary complexity of traditional models.
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Real-World Evidence
Relevant clinical data from actual product use.
We specialize in real-world-based studies and hybrid models that reflect how products are used in clinical practice and by consumers. We combine scientific rigor and operational flexibility to generate safety, performance, and clinical benefit data aligned with regulatory and market expectations.
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Support for Researcher-Initiated Studies
We transform clinical questions into actionable studies.
We support researchers, institutions, and clinical groups in the development and execution of investigator-initiated (IIT) studies. We offer methodological, regulatory, and operational support to transform clinical hypotheses into viable protocols, ensuring scientific quality, operational feasibility, and an appropriate structure for generating reliable evidence.
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Comprehensive Access and Regulatory Support Programs
Approval and implementation of special access programs
We plan and conduct regulatory approvals for expanded access and compassionate use programs, ensuring their implementation and ongoing management. We monitor participant safety, report adverse events, and ensure the proper submission of reports and documentation to regulatory authorities.
