InClymb ClinicalbyMalan Bosman·Aug 19, 2025Is this the future of TFL programming?This is the story of Steve, a Statistical Programmer tasked with programming the Tables, Figures and Listings (TFLs) for the CSR of a large…
Melanie Logan·Jul 20, 2025We Had the Blueprint the Whole Time: Why Clinical Data Hasn’t Automated (Yet)This article explores how the CDISC Operational Data Model (ODM) — often underutilized — could be the missing infrastructure layer in…
Yama F Mujadidi·Apr 4, 2025Managing Incomplete Dates in Clinical Trials: CDISC-Compliant Strategies, CRF Design and…Incomplete date capture — such as when only the month or year of an event is known — remains a persistent challenge in clinical research…
Tamer Chowdhury·Sep 12, 2023Building FAIR Data Products from Clinical Studies with CDISC Biomedical Concepts
Formedix·Aug 16, 2023What CDISC standards are used in clinical research? | FormedixThe Clinical Data Interchange Standards Consortium (CDISC) is dedicated to helping improve medical research through data standardization…
Formedix·Jul 19, 20233 key facts about ADaM standards in clinical trialsOne of the most important standards when it comes to clinical trial submission is the Analysis Data Model (ADaM). ADaM standards outline…
Formedix·Jun 21, 2023Streamlining Drug Development: the Role of CDISC StandardsThe clinical trial process is a long, expensive, complicated one that often ends in failure. That means to have a successful outcome…
Christian Baghai·Apr 20, 2023Establishing Traceability in FDA Reviews through the Use of CDISC Standards, SDRG, and ADRG: A…Introduction
Christian Baghai·Apr 20, 2023Optimizing Clinical Trial Data Submissions: Ensuring Consistency and Compliance with CDISC…1.Introduction
Christian Baghai·Apr 2, 2023Navigating Pinnacle 21 Reports: Best Practices for Handling Errors, Warnings, and NoticesIntroduction Clinical data is submitted to regulatory agencies for review during the drug development process. The Clinical Data…
