The CDISC US Interchange hybrid event provides an opportunity to network and know about the best practices in clinical data standards implementation and associated value. The October 2021 iteration will focus on key industry themes, including Analysis Data Model (ADaM), real-world data, the impact of COVID-19 on decentralized clinical trials (DCTs), CDISC standards, COVID-19 vaccine development, and CDISC 360 among other industry-mapped topics.
Implementation of a Metadata Repository (MDR)
Clinical standards initiatives and regulations have driven the need for defining standards across all functions of clinical trial activities. However, to create a holistic solution that enables governance teams to effectively track standards and aid study teams during setup, conduct, and analysis, one must consider the creation of metadata repository (MDR) along with all necessary functionalities. At the event, the speakers will elaborate on the value adds that organizations benefit from with the implementation of an MDR solution as well as the challenges that may arise during the implementation phase.
- Charusheela Thakur, Domain Consultant, ADD Data Standardization and Biometrics, TCS
- Jeannine Hughes, Senior Associate Director, Clinical Data Standards, Boehringer Ingelheim
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