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Real-World Evidence

What is Real-World Evidence?

Real-world evidence (RWE) refers to clinical data gathered outside the controlled environment of randomized clinical trials. It is derived from real-life data sources, such as patient registries, electronic health records (EHR), claims databases, and observational studies. This gives us insights that reflect how treatments and interventions perform in day-to-day practice.

Our RWE solutions generate insight that drives decisions. As a dermatology and aesthetic medicine CRO, we specialize in producing clinically relevant RWE that elevates product credibility, supports regulatory submissions, and strengthens market positioning.

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Why is RWE Essential?

Demonstrate effectiveness across varied populations

Monitor long-term safety

Support label expansions and market access

Provide evidence for clinical and economic value

What are the data sources for RWE generation?

Electronic health records (EHRs)
Claims and billing databases
Disease and adverse events registries
Patient-reported outcomes (PROs)
Observational studies

Setting the Standard in RWE

We build real-world evidence programs that meet the highest standards in regulatory, clinical, and practical relevance in dermatology and aesthetic medicine. 

Our Capabilities

Observational Study Design

Designed protocols for retrospective or prospective cohorts for publication, regulatory alignment, and real-world relevance.

Site and Investigator Network

We partner across hospitals and clinics throughout Saudi Arabia and the GCC. We manage the center and PI to collect the RWE data.

Data Management

We employ data capture software that is optimized for real-world workflows, and we implement robust data cleaning protocols, real-time discrepancy tracking, and continuous quality monitoring.

Statistical Analysis

Our statistics team are experienced in advanced real-world methodologies including time-to-event analysis, propensity score matching, sensitivity analysis, and more. 

Medical Writing and Dissemination

We transform real-world findings into impactful, publication-ready documents for peer-reviewed journals, regulatory submission, or conference material.

Regulatory Navigation

From site ethics submissions to regulatory submission we guide your RWE study through every step. Our team ensures that your RWE strategy aligns with both local regulations and global standards. Learn more about our Regulatory Affairs. 

Get in touch to request a quote or for more information about our RWE solutions.

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