Search Results: regulatory – Page 2

The enterprise AI platform accelerating systematic literature review with clinical-grade precision

Precision-first automation that reduces SLR timelines from months to days - without sacrificing rigor, auditability, or control.

Refining ambient AI for behavioral health with precise clinical terminology

Ambient scribes are surfacing across healthcare, including specialty fields like oncology and psychiatry. Learn why they need clinical grounding to scale.

How the IMO Health Platform structures clinical data across healthcare

Explore the intelligence framework making clinical data usable across healthcare, from EHR workflows to evidence generation to health tech innovation.

IMO Health Platform

IMO Health Platform Precise clinical data for modern health tech use cases Every major EHR trusts IMO Health’s foundational context 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

[ POINT OF CARE WORKFLOW ]

[ DATA QUALITY MANAGEMENT ]

Search Results: regulatory – Page 2

[ POINT OF CARE WORKFLOW ]

[ DATA QUALITY MANAGEMENT ]