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arw A Unique Propositions for CROs

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CEO Mark Wheeldon shares his thoughts on pharma outsourcing and how Formedix can support its growth in The Clinical Oncologist Daily interview.

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arw Define-XML 1.0 Nearing End of Life

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In March 2017, Define-XML 1.0 will no longer be supported by the FDA and will be replaced by Define 2.0. Discover hints and tips for the move to Define 2.0.

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arw Submission Ready Datasets 60% Faster

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Formedix launches automated service to convert datasets exported from EDC systems to CDISC SDTM format ready for FDA submission.

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Companies using Formedix save time and money...

 

The numbers speak for themselves:

  • 68% reduction in study set-up
  • 55% reduction in EDC build time
  • 23% reduction in resource
  • 70% content reuse across all clinical trials.

CDISCLogos

For the past 15 years, we have been working with CDISC and are proud to offer software, services and online training based on CDISC standards. We are a CDISC Registered Solutions Provider and our software has ODM Certifications.

Formedix Solutions

Formedix Origin - Universal Design

Formedix Origin

Origin is our flagship suite of productive universal study design tools for library development and creation of clinical trial designs.

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Formedix Transform - Universal Execution

Formedix Transform

Transform is our suite of universal execution tools for study build across multiple platforms, (EDC, ePRO, IVRS) and vendors, all from one tool.

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Formedix Control - Universal Compliance

Formedix Control

Control is our suite of universal content and design verification tools. It validates dataset metadata against standards and specifications against implementations.

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Formedix Consult - Universal Expertise

Formedix Consult

Consult is our portfolio of professional services for planning, preparation and implementation of all your CDISC and multi-vendor EDC implementations.

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