We will speak at this conference where buyers meets companies that provides medical devices!
Read more and secure your seat (zoom) here
We will speak at this conference where buyers meets companies that provides medical devices!
Read more and secure your seat (zoom) here
Swedish Medtech have several podds about medical devices in general but also a few specfic ones discussing the new regulations with Peter Löwendahl from Hoff&Lowendahl. These can be found here. Today we recorded a new Podd that will be released soon!
This 2 day course gives you deeper insight in clinical evaluation and clinical trials for medical devices. It will be online. Find out more about the course here.
In cooperation with Swedish Medtech we invite you to participate in this popular training. We will go yhtough all aspects on responsibilities, cover differences between countries and what to look out for. Ensure to get your seat reserved today through this link. This training will be online.
This seminar is about Post Market Surveillance. We will specific talk about how to meet the obligations in MDR and IVDR and not violate GDPR. For many manufacturer it might be a balance act to meet both at the same time. In the seminar the basic parts in the regulations will be reviewed and what you should think about!
Read more about the event and reserve your seat here. The seminar will be online.
We talk at the AIDA days about MDR, effects on research and things to consider with AI products. AIDA is supporting research. Read more here.
Peter Löwendahl was interviewed in the Swedish newspaper regarding Digital Health in Sweden. The article mainly covered software, MDR and Notified bodies.
If you want to read more about this, follow the link to Digital Hälsa
Hoff&Lowendahl has been named as one of the few companies in the region that have been able to drive both revenue, profit and hired people during the last year! Overall the workload for regualtory consultants have increased mainly due to IVDR and MDR says the CEO Lisa Lundström Löwendahl.