“CE” MARKED ON MOBILE APPLICATIONS

Nowadays the use of Smartphones and tablets are very common for the medical sector to inform patients. Diagnostics, treatments and follow-ups are revolutionizing the medical and patient relationship in many disciplines such as diets.

In the European framework, devices and applications that we have mentioned must meet the requirements of directives and regulations for medical devices. In this case, it is mandatory to have the health product manufacturer’s license, granted by the Agencia Española de Medicamentos y Productos Sanitarios. (AEMPS)

At QUALITYLINE: REGULATORY, CONSULTING & TRAINING we will accompany and train you to comply with European CE marking regulations , complying with all the functionalities for clinical safety in applications and devices in the healthcare market.