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Urgent Need to Revise the Medical Devices Regulation
by
chemsafe
|
29 October 2024
29 October 2024
|
Blog
,
Medical
The resolution on the urgent need to revise the Medical Devices Regulation, presented by several...
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Labelling of Cosmetic Products in the United States
by
chemsafe
|
24 September 2024
1 October 2024
|
Blog
,
Medical
In the United States, cosmetic products must comply with specific labeling requirements mandated by the...
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Clinical Evaluation of Orphan Medical Devices
by
chemsafe
|
9 July 2024
9 July 2024
|
Blog
,
Medical
What is a Orphan Medical Device? Orphan devices (ODs) are medical devices or their accessories,...
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MoCRA: How Chemsafe USA Can Secure Your Cosmetic Compliance
by
chemsafe
|
11 June 2024
11 June 2024
|
Blog
,
Medical
Modernization of Cosmetics Regulation Act (MoCRA) The publication of the Modernization of Cosmetic Regulation Act...
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Microplastic Ban: Impact on Medical Devices and Cosmetic Products
by
chemsafe
|
23 April 2024
23 April 2024
|
Blog
,
Medical
Starting from 17 October 2023, the EU will enforce a new regulation (COMMISSION REGULATION (EU)...
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Banned and Restricted Cosmetic Ingredients: What’s New
by
chemsafe
|
9 April 2024
8 April 2024
|
Blog
,
Medical
In last month, two amendments to Regulation (EC) 1223/2009 have been published: Commission Regulation (EU)...
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Global Cosmetic Regulations: a Brief Guide for the Complex Landscape of EU, UK, US, and China
by
admin
|
20 February 2024
21 February 2024
|
Blog
,
Medical
In a constantly changing cosmetic regulatory landscape, we have left behind a year full of...
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Regulatory Toxicology: Here’s how Chemsafe can help you
by
admin
|
30 January 2024
21 February 2024
|
Blog
,
Medical
,
Pharma
What is regulatory toxicology Regulatory toxicology is a particular branch of experimental toxicology, historically derived...
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EU reference laboratories for high-risk IVDs
by
admin
|
9 January 2024
29 January 2024
|
Blog
,
Medical
In a landmark decision, the European Commission, on December 5, 2023, has officially designated five...
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Prorogation for submission and authorisations of DEHP application for MD and IVD
by
admin
|
28 November 2023
29 January 2024
|
Medical
Where we stand with MDR and IVDR European regulations about Medical Devices (Reg. EU 2017/745)...
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