Latest News on Consumer Goods and Compliance

The advantages of a common charger for the EU market

The European Commission is working on a proposal featuring the idea of a common charger for several types of technological devices. Want to know more? Visit our page!

A professional uses an ultrasound machine

Use of Octylphenol ethoxylate (Triton-X-100) banned in medical devices and IVDs

The Commission Regulation (EU) 2020/2160 has restricted the use of Octylphenol ethoxylate in Medical Devices and In-Vitro Diagnostic Medical Devices from December 22, 2023, onwards. Want more details? Visit our page!

WEBINAR: UK SCPN COSMETIC PRODUCT REGISTRATION

In this webinar, we will provide an overview of the role of the Responsible Person in UK and the notification process

WEBINAR: PRODUCT INFORMATION FILE

In this webinar we will provide you with an overview about the definition of product information file and also the elements that must include

Legacy Devices and Certificates: Updates from BSI

The BSI announced in June of 2021 updates concerning certificates issued for medical devices. Do you want to know how these changes will affect manufacturers and their industries? Visit Our Website.

French CA issues procedure deal with risks of rupture of essential medical devices and IVDs.

The French CA together with the ANSM has published a management procedure to support the market operators and prevent a shortage of medical devices and in- vitro diagnostic devices.

IFRA Standards – 50th Amendment

The 50th amendment to the IFRA standard prohibits the use of one new fragrance ingredient. Discover more details in our article!

Person Responsible for Regulatory Compliance (PRRC) Seminars (MDR/IVDR)

Two-day seminar delivered by top industry experts! Aimed at providing basic knowledge and concepts to those who are interested in the role of Person Responsible for Regulatory Compliance (PRRC).