Medical

Urgent Need to Revise the Medical Devices Regulation
||,
The resolution on the urgent need to revise the Medical Devices Regulation, presented by several...
continue reading
Labelling of Cosmetic Products in the United States
||,
In the United States, cosmetic products must comply with specific labeling requirements mandated by the...
continue reading
Clinical Evaluation of Orphan Medical Devices
||,
What is a Orphan Medical Device? Orphan devices (ODs) are medical devices or their accessories,...
continue reading
MoCRA: How Chemsafe USA Can Secure Your Cosmetic Compliance
||,
Modernization of Cosmetics Regulation Act (MoCRA) The publication of the Modernization of Cosmetic Regulation Act...
continue reading
Microplastic Ban: Impact on Medical Devices and Cosmetic Products
||,
Starting from 17 October 2023, the EU will enforce a new regulation (COMMISSION REGULATION (EU)...
continue reading
Banned and Restricted Cosmetic Ingredients: What’s New
||,
In last month, two amendments to Regulation (EC) 1223/2009 have been published: Commission Regulation (EU)...
continue reading
Global Cosmetic Regulations: a Brief Guide for the Complex Landscape of EU, UK, US, and China
||,
In a constantly changing cosmetic regulatory landscape, we have left behind a year full of...
continue reading
Regulatory Toxicology: Here’s how Chemsafe can help you
||, ,
What is regulatory toxicology Regulatory toxicology is a particular branch of experimental toxicology, historically derived...
continue reading
EU reference laboratories for high-risk IVDs
||,
In a landmark decision, the European Commission, on December 5, 2023, has officially designated five...
continue reading
Prorogation for submission and authorisations of DEHP application for MD and IVD
||
Where we stand with MDR and IVDR European regulations about Medical Devices (Reg. EU 2017/745)...
continue reading