INFARMA is a European Pharmacy Meeting consisting of the European Congress of Community Pharmacy and the Medicine and Parapharmacy Exhibition.
Date:22-24th March 2022. Location: Madrid.
The new Regulation 2017/745 (EU) on Medical Devices (MDR) imposes strict demands on medical device manufacturers, Notified Bodies, and extends the scope also to the pharmaceutical industry related to medicinal substances with an integral medical device. Article 117 of the MDR amends the Directive 2001/83/EC, point 12 of Section 3.2 and requests for (single) integral products the involvement of a notified body to assess the conformity of the device part with the relevant general safety and performance requirements (GSPR) of Annex I.
Stefano Bolletta Sales Manager MHS Division of TÜV Italia will be present at INFARMA on Wednesday 23 March.
You can book an appointment with Stefano Bolletta by sending an email to this address: [email protected]