Full title: Emulating the Main Outcomes of Randomised Controlled Studies Through Statistical Analysis of Real World Data Directly Extracted from Electronic Medical Records.
Poster: Can real world data support drug development with better trial design and real-world evidence?
Our work with our partner Clinerion uncovers how use of statistical analytics methodologies on electronic health records can build synthetic control arms to supplement clinical trial data for better clinical and regulatory decisions.
Objective: To demonstrate that analysis of EMR can be used effectively to emulate patient and response patterns reflecting the results observed in randomized controlled trials (RCT).
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Your Benefits When Choosing Datametrix
Flexibility &
Connectivity
With offices in Switzerland (Neuchâtel), Sweden (Molndal at the AstraZeneca BioHub) and North Africa, we have always embraced virtual team working solutions and techniques. We connect rapidly and readily – through virtual media or in person.
Reliability & Expertise
Ensuring the delivery of your projects on time, to the expected standards and within budget, we have a team of highly qualified data analysts and biostatisticians with extensive experience and deep expertise.
Ability to Adapt
to Your Scope
Your needs come first. Our core skills are around data analytics, biostatistics, HEOR, data management and programming. Our large network or partners enables us to broaden our range of services, including clinical operations project management, field monitoring and site management.
Cost-Effectiveness to Compete
Datametrix’s lean management and efficient organization enables us to develop cost-effective solutions , helping you manage your budget challenges. If you are unsure about the amount of work that can be delivered at a certain budget, please reach out – our goal is to support you the more we can while fitting your budget.
For your data analysis needs, go with Datametrix.
In the past 18 years, we have worked with all kind of life science organizations – from global players to start up biotechs.
We understand your journey, regardless of the size of your team or company. This involves the growth of your pipeline, size and complexity of your studies, and hence the need to develop internal data standards, high quality processes and procedures. We are committed to partner on these as part as our FSP model. You will not be left with just a trial result report, but also with internal capabilities, standards and processes. This ensures that you will remain both compliant and in control of subsequent steps of your development and growth path.
We would be happy to assess your needs together. Book a call with us, or drop us an email.
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