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WHO WE ARE
The eClinical Forum is a global network of peers. It provides a non‐competitive environment for innovation, learning and collaboration in clinical research.
eCF Submission to EMA on their Reflection Paper on the Use of IRT (Interactive Voice/Web response Systems in Clinical Trials)
Practical Considerations for Clinical Trial Sites using Electronic Health Records (EHRs) certified for Clinical Research
Leveraging EHR Data to Improve Clinical Research - Informa Brussels 25May11
eCF comments on FDA Draft Guidance: Electronic Source Doc in Clinical Investigations
Re-use of Electronic Health Records for Clinical Research
The EHRCR Functional Profile Working Group is comprised of dedicated individuals from the United States and the European Union in the following industries: pharmaceutical, biotechnology, clinical research technology vendor, healthcare technology vendor, and federal regulator.
As the healthcare and pharmaceutical technology spheres move closer together at the clinical research interface, the eClinical paradigm needs to be revisited in order to leverage emerging political, cultural, procedural and technological opportunities. Understanding investigational site experiences with today’s clinical trial technologies and their perspectives on future requirements is critical to delivery of improved eClinical solutions
2009: EHRCR User Requirements Addendum, Draft 2, 16 April 2009
2009: HL7 EHR Clinical Research Functional Profile, Release 1
Please download to review these comments.
Please download to review this document.
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eCF Spring Workshop in Ridgefield, Connecticut USA
Registration is open for the eCF Spring Workshop, kindly hosted by Boehringer Ingelheim at their Ridgefield, Connecticut campus on April 30 to May 3, 2024.