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L'etichetta è l’elemento più importante del packaging cosmetico e viene regolarmente supervisionata dalle autorità regolatorie...

Biocides: BPC approves Ethanol use for disinfectants and hand sanitizers On February 24 in Helsinki,...

by Gabriele Pincitore|24/02/202626/02/2026|Blog, Pharma

Permitted Daily Exposure (PDE, also referred to as “permissible daily exposure”) is a health-based limit...

The European Database on Medical Devices, a key element of the European Union’s regulatory framework...

What are PFAS? The large family of synthetic substances is characterized by the presence of...

Medical Devices: FDA’s SaMD Clinical Evaluation Guidance withdrawn The FDA revised its guidelines in 2026...

by Gabriele Pincitore|27/01/202605/02/2026|Blog, Food

In the European Union, food additives can be used in food and beverages only if...

Clinical evaluation remains one of the most critical and challenging elements of medical device compliance....

ECHA’s body, the Forum for Exchange of Information on Enforcement (the Forum) has adopted its...

The EU Medical Device Regulation (MDR, EU 2017/745) defines the regulatory framework for the design,...