Rogans Medical Research
ROGANS S.A.S. is a healthcare provider institution (IPS) founded in 2021, with a clinical and operating model designed to strategically support clinical research
Operating across multiple sites
General medicine, dermatology, psychiatry, internal medicine and clinical nutrition.
Our own clinical infrastructure, with home medical care and virtual tools including tele-guidance, teleconsultation and telemedicine.
A hybrid care model that makes recruitment easier
Leading institutions in other medical specialties that significantly expand the diversity and size of the populations available for clinical studies, especially in low- and medium-complexity research.
The organization runs structured recruitment funnels, population segmentation processes and preliminary pre-screening activities aimed at identifying viable candidates according to the criteria defined in each protocol. These processes are always carried out under the guidelines of the research site, the sponsor and the relevant ethics committee.
Information is handled securely and traceably, and limited to what is strictly necessary, so it can be forwarded in a controlled way to the research site for the next stages of the study.
ROGANS's experience has focused mainly on Phase IV clinical research and observational studies, as well as on supporting research sites in ways that directly affect the speed, efficiency and feasibility of enrollment.
At the same time, the organization is strengthening and aligning its processes with Good Clinical Practice (GCP) standards, with the goal of gradually expanding its role as a strategic partner in Phase I to III studies, always as a collaborative complement to the principal research site.
ROGANS has the experience and capabilities to help identify, approach and engage sponsors, both in Colombia and internationally, including strategic partners and contacts in the United States.
This support aims to facilitate preliminary connections, provide information on population feasibility and recruitment capacity, and take part in early discussions, always in coordination with the research site and under the applicable confidentiality agreements.
The organization runs structured recruitment funnels, population segmentation processes and preliminary pre-screening activities aimed at identifying viable candidates according to the criteria defined in each protocol. These processes are always carried out under the guidelines of the research site, the sponsor and the relevant ethics committee.
Information is handled securely and traceably, and limited to what is strictly necessary, so it can be forwarded in a controlled way to the research site for the next stages of the study.
ROGANS's experience has focused mainly on Phase IV clinical research and observational studies, as well as on supporting research sites in ways that directly affect the speed, efficiency and feasibility of enrollment.
At the same time, the organization is strengthening and aligning its processes with Good Clinical Practice (GCP) standards, with the goal of gradually expanding its role as a strategic partner in Phase I to III studies, always as a collaborative complement to the principal research site.
ROGANS has the experience and capabilities to help identify, approach and engage sponsors, both in Colombia and internationally, including strategic partners and contacts in the United States.
This support aims to facilitate preliminary connections, provide information on population feasibility and recruitment capacity, and take part in early discussions, always in coordination with the research site and under the applicable confidentiality agreements.
ROGANS has a solid, interdisciplinary research team with experience in clinical research, regulation, ethics and regulatory compliance:
These are some of the professionals behind our clinical research, ethics and regulatory compliance processes
Researcher with a doctorate in Biological Sciences (Translational Medicine) and more than ten years of experience in clinical research, pharmaceutical development and regulated products. He has taken part in Phase I-II clinical trials, randomized double-blind studies, toxicology assessments, and oncology and translational medicine research. He has multiple peer-reviewed scientific publications and experience in regulatory strategy and in preparing scientific dossiers for national and international health authorities. He provides expert support in study design, clinical validation and evidence-based product development.
Research bacteriologist with experience supporting clinical research processes, analyzing scientific information and providing technical support for health studies. He works on data management, quality control, monitoring of analytical processes and operational support for research projects, contributing to the traceability and reliability of clinical information.
Researcher with extensive experience in regulatory compliance, Good Clinical Practice (GCP) and health regulation. She has a track record in procedures before INVIMA (Colombia's drug regulatory agency) and local health departments, as well as in helping healthcare institutions with licensing, audits and stronger quality systems, ensuring compliance with regulatory and ethical standards in clinical research.
Psychologist with experience in patient assessment, support and follow-up, as well as in clinical research support processes. Her role focuses on the psychosocial care of participants, contributing to adherence, well-being and appropriate interaction throughout clinical studies.
Researcher with extensive experience in regulatory compliance, Good Clinical Practice (GCP) and health regulation. She has a track record in procedures before INVIMA (Colombia's drug regulatory agency) and local health departments, as well as in helping healthcare institutions with licensing, audits and stronger quality systems, ensuring compliance with regulatory and ethical standards in clinical research.
Physician specializing in dermatology, with clinical experience in the evaluation, diagnosis and management of skin conditions. She provides clinical support for dermatology-related research studies, contributing specialized medical judgment and support in participant evaluation.
A team specializing in health service licensing processes under Colombia's Resolution 3100 of 2019. They provide support with regulatory compliance, document management and verification of licensing standards, ensuring that clinical operations meet current regulatory requirements.
Research nurse with experience in clinical care and operational support for research processes. He takes part in patient follow-up, procedure support, data collection and clinical coordination, contributing to the safe and orderly conduct of studies.
ROGANS coordinates its research processes with an external, independent Research Ethics Committee, Riesgo de Fracturas S.A., which is pluralistic and interdisciplinary. This committee reviews research protocols and issues ethical opinions on them, protecting the rights, safety and well-being of participants in line with the national and international ethical principles that apply to research involving human subjects.
This team allows ROGANS to bring together its clinical, scientific, ethical and regulatory capabilities in a comprehensive way.
We act as a third-party partner that complements the capabilities of the research site, without replacing its clinical, scientific or regulatory role.
Our value proposition is built on our ability to combine:
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