GTF MCAMPS BLOG

HT Cluster organises HealthTech Unconference Event 2017

23 Nov, 2017 | News, Medical devices

HealthTech Unconference Event 2017 HealthTech Cluster

The HealthTech Cluster is organising its annual meeting today, 23 November. HealthTech Unconference Event 2017. This conference, which is being held in Sabadell, uses the methodology unconference, This method also allows all attendees to participate in the co-creation of the content. This method also allows all attendees to participate in the co-creation of the content. Do you want to know what we are going to talk about?

The HealthTech Unconference Event 2017 Programme

The programme The day starts at 9 a.m., when attendees are welcomed and participants are introduced. From 9.30 a.m. onwards, a cycle of 3 simultaneous round-table discussions begins with a moderator. Each attendee must decide which of the 3 is of most interest to them.

Throughout the day, there will be talks on big data, medical devices, bioethics, healthcare applications, biomaterials and artificial intelligence... And all attendees will participate in the creation of the content of each conference.

At 17h, the conclusions of the Unconference will be presented to the public. And finally, 2 activities in which all the partners participate: a brief presentation of each of the attendees and the company they represent, and a talk on innovation and challenges proposed by the cluster companies.

To end the day, the Health Tech Cluster proposes a drink with the partners participating in the HealthTech Unconference Event 2017.

HealthTech Unconference Event 2017 HealthTech Cluster Mercè Camps Manel Pretel

GTF participates in HealthTech Unconference Event 2017

The director of the Technical Pharmaceutical Office, Mercè Camps, The event was organised at the Molí de Sant Oleguer sports centre. There, he coincided early in the morning with Manel Pretel, director of the HealthTech Cluster. In addition, Camps has actively participated in the talks on medical devices. In them, she offered her point of view as an expert on the regulation of medical devices and the new PS and IVD Regulation.

 

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