Learn How to Maximize Vault Performance
Learn How to Maximize Vault Performance
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Register HereKey Topics for 2025:
The future of medical device trials is being built on interoperable, high-quality data. In an effort to streamline processes and accelerate innovation, the Medical Device Innovation Consortium (MDIC), in partnership with the Clinical Data Interchange Standards Consortium (CDISC) and the FDA, is leading an initiative to develop data standards for in vitro diagnostic (IVD) devices.
This session, led by clinical data experts, will highlight the significant progress being made. The panel will share key insights from the recently published landscape analysis and discuss:
Join us to learn how these standardization efforts are creating an end-to-end harmonized platform that will shape the future of clinical trials for IVDs.
Speakers:
Moderator:
Presented by: MDIC, Veeva MedTech, and CDISC Organized by: Medical Device Innovation Consortium
Learn More & RegisterMedical Affairs is evolving and enabling fast, compliant, strategic engagement with HCPs and KOLs. Connectivity across channels is imperative to get products to patients and to understand their needs.
Join this webinar for insights on:
Ascensia Diabetes Care, Global Program Lead, Ntianu Onumonu will share how the company implemented a claims and content management program that reduces review and approval times, enhances compliance, and streamlines marketing operations.
Ntianu will share:
João Martins, Associate Director of Regulatory Affairs Strategy at Abbott, and Megha Deviprasad Iyer, Director of Global Strategic Regulatory Affairs at Thermo Fisher Scientific will address the growing challenges for regulatory affairs professionals amid increasing global health regulations and shifting priorities.
They will discuss: