
COSMOS
Scientific
Medical Affairs Services
At COSMOS Scientific, Inc., we provide comprehensive Medical Affairs services to support pharmaceutical and medical device companies throughout the product lifecycle. Our offerings help you generate, communicate, and apply scientific and clinical evidence with clarity and impact.
Medical writing
We provide high-quality medical writing services to support your scientific and regulatory needs. Our team produces a wide range of documents, including case reports, review articles, clinical practice guidelines, consensus, abstracts, posters, and patient-oriented materials.
Advisory Boards
COSMOS Scientific organizes and facilitates expert advisory boards to gather clinical insights and strategic guidance. We manage the end-to-end process—from identifying key opinion leaders (KOLs) to coordinating meetings and generating actionable summaries—to help refine your clinical development and commercialization strategies.
Expert Consensus Programs
When evidence is limited or evolving, we facilitate expert consensus panels to generate structured opinions that can guide clinical decision-making and policy. Our team manages the process using Delphi methods, nominal group techniques, or other validated approaches to ensure scientifically sound results.
KOL Mapping and Engagement
Our KOL identification and engagement services help you connect with the right experts to drive scientific collaboration and product advocacy. We analyze influence networks, map stakeholder landscapes, and build engagement strategies that align with your medical goals.
Clinical Practice Guidelines Development
We support the development and update of evidence-based clinical practice guidelines in collaboration with academic leaders and medical societies. Our role includes literature reviews, expert panel coordination, methodology design, and editorial oversight, ensuring credibility, transparency, and impact.
Real World Evidence (RWE)
At COSMOS Scientific we specialize in the design, generation, and analysis of Real World Evidence (RWE) for medical devices, pharmaceuticals, and biotech innovations across Colombia and Latin America. We harness real-world data from routine clinical practice—such as electronic health records, patient registries, claims databases, and digital health platforms—to assess effectiveness, safety, utilization patterns, and long-term outcomes beyond controlled clinical trial settings. Our work combines scientific rigor, regulatory alignment, and operational excellence to deliver actionable insights that support market access, post-marketing commitments, health economics, and evidence-based decision-making throughout the entire product lifecycle.