New to CDISC - Technology/Software Developer
cdisc.org
New to CDISC - Technology/Software Developer
As clinical studies become more complex, the need for clarity in the data is increasingly important. That’s why we work with a wide range of experts to develop standards that provide a common language that’s interoperable among systems across the clinical research lifecycle.
Sep 6, 2018
Clinical Data Interchange Standards Consortium Clinical Data Standards
Dr Raghav on Data Interpretation Standards in ctDNA CRC Clinical Trials | OncLive
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Clinical data management runs on precision. One error can delay approvals. Terminology protects trial integrity. This guide explains CDM essentials by: • Clarifying GCP and ICH requirements • Explaining audit trail standards • Strengthening query management • Supporting inspection readiness • Improving submission timelines For CDMs, this builds authority. For sponsors, it protects data quality. Compliance starts with language. Read the full article here: 🔗 https://ccrps.org/clinical-research-bl
0:29
Clinical data management runs on precision. One error can delay approvals. Terminology protects trial integrity. This guide explains CDM essentials by: • Clarifying GCP and ICH requirements • Explaining audit trail standards • Strengthening query management • Supporting inspection readiness • Improving submission timelines For CDMs, this builds authority. For sponsors, it protects data quality. Compliance starts with language. Read the full article here: 🔗 https://ccrps.org/clinical-research-bl
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