Search Results: regulatory – Page 2

IMO Health Platform

IMO Health Platform Precise clinical data for modern health tech use cases Every major EHR trusts IMO Health’s foundational knowledge layer, now

Why drug repurposing requires biomedical NLP and AI

Learn how NLP and generative AI are enhancing drug discovery and repurposing by extracting insights from complex biomedical data.

ICD-10-CM 101: A guide to the international coding system

Need a refresher on why the ICD-10-CM system is an important part of clinical documentation? Our 101 guide breaks it down.

FDA issues first guidance on AI in drug development

The FDA has provided direction on the use of AI for drug and biologic development. Here’s what life sciences teams should know.

Top health IT news stories from December 2025

Before we head into the new year, let’s reflect on some of the most significant news stories in health tech from December

Denials management

Denials management Reduce denials, write-offs, and retrospective coding Stop revenue loss before it starts with proactive upstream and downstream denials management. schedule

Active documentation as a revenue strategy in 2026

Hospitals are losing millions to rising costs and incomplete documentation. Learn how precise terminology can prevent costly denials and protect revenue.

Standardizing for scale: A blueprint for real-world data excellence

Learn how Norstella automated code updates, reduced onboarding and cleansing time, and decreased manual labor costs by partnering with IMO Health.

USCDI V3 compliance is mandatory by 2026 – here’s how to get ready

The addition of USCDI V3 and V4 to IMO Health’s proprietary lexicon ensures health systems comply with rapidly evolving regulations, avoiding costly

NDC codes 101: A complete guide to National Drug Codes

The U.S. government uses the National Drug Code (NDC) to identify and track drugs intended for human use. Get up to speed

How can ambient AI scribes capture clinical nuance?

Ambient intelligence tools are skilled at recording patient-provider encounters in real-time. But can they truly understand them?

Rethinking literature reviews with AI and clinical terminology

Pharma’s SLR workflows are slow, costly, and error-prone. See how AI and clinical terminology accelerate evidence generation with precision and trust.

POINT OF CARE WORKFLOW

DATA QUALITY MANAGEMENT

Search Results: regulatory – Page 2

POINT OF CARE WORKFLOW

DATA QUALITY MANAGEMENT