Raiana Word Add-in V2 Update | Smarter AI, Faster Document Understanding & In-Doc Chat History
Raiana Word Add-in V2 Update | Smarter AI, Faster Document Understanding & In-Doc Chat History The Raiana Word Add-in has been upgraded to version 2, bringing powerful new capabilities directly into Microsoft Word. In this update walkthrough, Raiana co-founder Erik Vollebregt and full-stack developer Sajitha Dissanayake demonstrate how the add-in now delivers a more seamless, […]
Raiana Standards Apps: Checklist Generation & AI Gap Analysis (Pro & Enterprise Demo)
Raiana Standards Apps: Checklist Generation & AI Gap Analysis (Pro & Enterprise Demo) In this demo, the Raiana team introduces two powerful standards-based applications available for Pro and Enterprise users: the Standard Checklist Generator and the Gap Analysis tool. Together, these tools help regulatory and compliance teams turn complex standards into structured, actionable outputs and […]
Raiana How-To with Nancy Hu: Introducing Raiana Verify | AI-Assisted Response Verification
Raiana How-To with Nancy Hu: Introducing Raiana Verify | AI-Assisted Response Verification & Custom Instructions We’re introducing Raiana Verify, an AI-assisted verification feature designed to add an extra layer of confidence to your regulatory workflows. With Raiana Verify, a second independent AI reviews and checks Raiana’s responses, helping you validate outputs and strengthen the human-in-the-loop […]
Raiana How-To with Nancy Hu: Word Add-in | Write, Review & Chat in Microsoft Word
Raiana How-To with Nancy Hu: Word Add-in | Write, Review & Chat in Microsoft Word & Custom Instructions Discover how the Raiana Word Add-in integrates powerful AI directly into Microsoft Word. In this walkthrough, Nancy Hu demonstrates how to review document sections, ask follow-up questions, and generate context-aware writing without ever leaving Word. From drafting […]
The Augmented Professional Ep. 2 | Michael Konings: Modernising RA & Building an AI-Ready Team
The Augmented Professional Ep. 2 | Michael Konings: Modernising RA & Building an AI-Ready Team How will AI reshape Regulatory Affairs, and what skills will tomorrow’s regulatory professionals need? In the second episode of The Augmented Professional, Thomas Meerts speaks with Michael Konings, Head of Regulatory Affairs IGT-S at Philips, about the future of AI […]
Raiana How-To with Nancy Hu: MyRaiana | Save Product Information & Custom Instructions
Raiana How-To with Nancy Hu: MyRaiana | Save Product Information & Custom Instructions Save time by personalizing your Raiana experience with MyRaiana. In this tutorial, Nancy Hu demonstrates how to use MyRaiana to securely store your company and product information, eliminating the need to repeatedly describe your products in every new chat or application. You’ll […]
How to Install the Raiana Microsoft Word Add-in | Step-by-Step Guide
How to Install the Raiana Microsoft Word Add-in | Step-by-Step Guide Integrate Raiana directly into Microsoft Word and access Regulatory Augmented Intelligence without leaving your document. This step-by-step tutorial shows you how to install and start using the Raiana Word Add-in, allowing you to streamline regulatory writing and documentation directly within Microsoft Word. This tutorial […]
The Augmented Professional Ep.1 | Regulatory AI in QMS: Hallucinations, Validation & Risk Explained
The Augmented Professional Ep.1 | Regulatory AI in QMS: Hallucinations, Validation & Risk Explained How should regulatory teams use AI inside a Quality Management System (QMS)? And why are hallucinations one of the biggest concerns in regulatory AI? In this episode of The Augmented Professional, we break down how AI tools can be safely integrated […]
Is Your Software a High-Risk AI System? Here’s the fastest defensible way to find out.
Is Your Software a High-Risk AI System? Here’s the Fastest Defensible Way to Find Out. It usually starts with one product, one deadline, and six documents open at once: the AI Act’s Article 6(1) criteria, the MDR or IVDR technical documentation, the harmonized standards, the risk file, last year’s classification memo, and a message from Engineering asking […]
The Capacity Gap No One’s Naming in Regulatory Affairs
The Capacity Gap No One’s Naming in Regulatory Affairs On average, a new or revised national regulatory document relevant to medtech is published every 53 minutes worldwide. ¹ This frequency transforms staying up to date from a discussion point into a staffing challenge that traditional organizational structures are not equipped to manage. This is not a knowledge gap. The real […]
