Service Portfolio
RMMEGS presents a comprehensive suite designed to facilitate evidence excellence.
From Question to Evidence.
End-to-end support for real-world evidence generation — from the first research question to the final deliverable. Engage us for a single work package or the full study lifecycle.
Study design & execution
Observational and real-world study design grounded in validated methodologies — comparative effectiveness, external control arms, and post-authorisation safety studies (PASS).
Clinical algorithm development & validation
Cohort definitions, therapy algorithms, and clinical coding tailored to the structure and clinical practice behind each database.
Data analysis & output
Analysis of large-scale real-world data — EMRs, administrative claims, and clinical registries — with clear, decision-ready outputs.
Protocol & SAP writing
Authoring and review of study protocols and statistical analysis plans, aligned with your research goals, the literature, and regulatory expectations.
Regulatory-grade RWE
Evidence generation built to the standard regulators expect — from feasibility assessment through analysis, interpretation, and reporting.
Pharmacoepidemiology & Pharmacovigilance
Advanced epidemiological and statistical methods applied to safety and effectiveness questions across diverse therapeutic areas.
Vendor & stakeholder management
Selection and oversight of external vendors and research partners, keeping deliverables on quality, on time, and on budget.
Literature reviews & evidence gaps
Systematic literature reviews and evidence-gap assessments to position your study within the current landscape and unmet needs.
How it works:
Get in touch.
Complete the inquiry form to discuss tailored study solutions and receive a detailed proposal within three business days.