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INDUSTRY
SESSION

Session dedicated to company operators

of the Aesthetic Medicine sector.

Representatives of the operators will be present

and the institutions of the sector

INTERVENTIONS -

Introduction and moderation of the session by Agorà Legal Office

Claudio Plebani, Martina Bianco

How to submit a clinical investigation to begin the medical device certification process: from validation to authorization.

Eng. Michela Maggi - Ministry of Health - Office 6 "Clinical trials and investigations"

CE certification of products with aesthetic purposes as medical devices pursuant to EU Regulation 2017/745

Eng. Alessandra Basilisco - Ministry of Health - Office 3 "Medical Devices and Active Implantable Medical Devices"

Fernanda Gellona intervenes -

General Manager Confindustria Medical Devices

Answering questions and discussion

with the companies in the sector present

PARTICIPATION IS FREE
FOR EXHIBITORS REGISTERED FOR THE CONGRESS.

For non-exhibiting companies, participation
is available with “Industry Delegate” registration.

WE INVITE COMPANIES TO SHARE ANY QUESTIONS OR SPECIFIC TOPICS THEY WISH TO BE DISCUSSED DURING THE SESSION BY WRITING AN EMAIL TO LEGAL@SOCIETAMEDICINAESTETICA.IT

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