Generate insights from Real World Data for your research

Billions of clinical facts with unique RWD ecosystem

20+ countries

700+ research sites

1 000 000+ EHR

TALK TO OUR TEAM

A member of

Access to patient data from all over the world

60M+

Electronic Health Records

30+

Global locations

Data coverage

Germany, The United Kingdom, Spain, Portugal, The Netherlands, Switxerland, Czechia, Slovakia, Belorus, Russia, Canada, USA, Turkey, United Arab Emirates, Israel, Saudi Arabia

Harnessing and transforming RWD into RWE

Real-World Evidence for complex healthcare decision making

Combining data, AI-technology,
and analytics to empower your trials

01. Real-World Data Provider

Collection, processing, and harmonization of unstructured data using algorithms, which are quickly adapted for a particular task. We provide curated datasets to answer your research questions.

02. AI for data extraction

Deep Learning techniques for the extraction of medical information including entity recognition and relation extraction. We deliver AI-powered algorithms for evidence representation.

03. Clinical Research Company

End-to-end solutions including study design, feasibility, patient recruitment and final reports.

04. IT Solutions Developer

Deployment of customized web tools for healthcare professionals, patients, and sponsors.

Solutions for your specific clinical trial needs

Delivering cutting-edge
RWE insights

1 000 000+
electronic health records

Services

01

Real World Evidence Solutions for your Study

Epidemics studies
"Smart" patient registry
Pharmacoeconomics studies
Marketing analysis of prescriptions
Drug treatment efficacy and safety
Post-authorization and additional studies

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02

Medical Writing

Development of a full document set for trial

Clinical study design
Clinical study protocol
Informed consent
Investigator’s Brochure
Clinical study reports
Articles and publications
Translation of documents

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03

Biostatistics

Scientific approach to study planning and data analysis
Sample size calculation
Development of the statistical section of study protocol
Statistical analysis planning
Randomization schedule development
Statistical data analysis
Presentation of results in TFLs with explanatory notes
Development of interim and final statistical report

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04

Pharmacovigilance

Set up of PVG specific processes and procedures
Collection, description and processing of serious adverse events data
Evaluation of safety data
Data entry and MedDRA coding
Medical review, quality control
Reporting to regulatory authorities and investigator sites about presumed serious and unforeseen adverse reactions (SUSAR)
Preparation and submission of annual safety reports to regulatory authorities and investigator sites

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Pharmacoeconomics studies

Modeling patient and healthcare system expenses on diagnostics and treatment
Determining RWD for modeling

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Products

01

Treatment analyzing tools

AI empowered predictive analytics tools for estimating patient survival based on Real-World Evidence extracted from Publications, Registries and Electronic health records.

The tool allows the estimation of the survival of a patient based on their individual parameters and performed or planned treatment, before being compared with the best treatment option for similar baseline data.

DM RWE creates Treatment Analyzing tools for any therapeutic area with complex and expensive treatment regimens

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02

Feasibility Tool

Estimate the capacity of RWD for your study with our online assistant, which delivers instant feasibility assessment based on the analysis of millions of electronic health records.

An intuitive user-friendly interface performs real-time analysis and enables preliminary estimation of whether presented datasets will fit your study goals. This will allow you to make an informed decision before making a purchase.

Reach out to one of our experts and find out how the Feasibility Tool brings together all the variables of compliant use to generate the evidence you are looking for.

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03

Datasets

Discover the potential of the global RWD derived from millions of electronic health records. With our broad network of healthcare organizations from EU, CIS, MENA and APAC countries, we collect large datasets in a avariety of therapeutic areas. We deliver clinically enhanced data for oncology and oncohematology, which combines histology, genomic data, biomarkers, treatment, line change, and survival records. Using Artificial Intelligence, DM RWE mines valuable datasets and provides clean and curated data to answer your research questions

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Data Source Validation Tool

We are committed to providing research-ready high quality data.

Our quality control system is designed in a way that requires all data to be checked for accuracy and suitability at every level of processing.

To that end we employ our special in-house designed automated Data Validation Tool.

You can order data validation by our team as a standalone service or deploy it on your own by acquiring it as a SaaS solution.

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What clients say about DM RWE

RWE Lead

Germany based biotech company

We’ve started working with DM RWE back in 2020. We’ve been more than happy with their delivery and performance. The team is very responsive, ethical and commited.

Head of Evidence Generation Projects

Pharmaceutical Company, Netherlands

We’ve been thoroughly impressed with the expanse of global patient data DM RWE has access to. But what’s important is that they work by the book and deliver utmost compliance and efficiency.