Gabriele Pincitore

Attending H3i 2026 as an Attendee and hosting a talk on CLP. 4 March 2026...

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...

Attending PestMed 2026 as an Attendee. 11 February 2026 in Bologna(Italy).

Medical Devices: FDA’s SaMD Clinical Evaluation Guidance withdrawn The FDA revised its guidelines in 2026...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