On Demand Webinar – Data driven content – FHIR and the future of Regulatory Submissions
Overview The shift to structured content and data has been a long-term objective for regulatory agencies and the Biopharma industry. However, progress has been hampered by a lack of open and broadly adopted industry standards and tools. While the Electronic Common Technical Document (eCTD) is a widely adopted standard for regulatory submissions, it only uses […]
Essential Guide to – FHIR (Fast Healthcare Interoperability Framework from HL7 )
Within modern healthcare technology, data interoperability has become a prominent topic across the field. As technology has continually improved, so has the ability to record healthcare data digitally. Electronic health records (EHRs) must be accessible across platforms for specified parties, while protecting data integrity. Seamless data exchange improvements are sought after in the field by […]