The Hase blogs
Regulatory, General
5 min
by Marc Chaillou
What most proofreading software gets wrong about compliance
FMCG
5 min
by Vineed Ravindranath
Beyond the warning label: a manufacturer’s guide to the 2026 U.S. labeling transition
Medical device
8 min
by Vineed Ravindranath
From review to approval: medical device labeling workflow
Pharmaceutical
5 min
by Dr. Jutta Hohenhoerst
Pharmaceutical labeling workflow: from clinical submission to printed packaging
Pharmaceutical, Medical device, Regulatory, FMCG
5 min
by Vineed Ravindranath
Multilingual labeling best practices: ensuring accuracy for global brands
Medical device, Regulatory
5 min read
by Marc Chaillou
The hidden complexity of global labeling: what medical device and IVD teams need to know
Regulatory, General
5 min
by Peter Muller
TVT vs generic proofreading tools: what regulated teams must know
Medical device, Regulatory
5 min
by Marc Chaillou
Medical device labeling standards: how to stay ahead of MDR and UDI
Regulatory, General
5 min
by Marc Chaillou
What is document comparison software in regulatory affairs?
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