News

One step closer to postpone the Medical Device Regulation (MDR)

One step closer to postpone the Medical Device Regulation (MDR)Last Friday, the European Parliament adopted the EU Commissions proposal on...

Proposal to postpone the MDR

March 25th the EU commission announced that they are working on a proposal to postpone the application of the Medical...

Theme day on MedTech Business Development

Last week Devicia held a presentation together with Clarvin on "The transfer process from MDD to MDR -...

How to transfer from MDD to MDR?

May 26th 2020 is rapidly approaching and we still awaits high impact guidelines. However, this does not mean that you...

The Journey of a MedTech Product

Do you want to learn more about the journey of a MedTech product through clinical evaluation and clinical investigation before...

MedTech Business Development with Läkemedelsakademin

On March 11th, Devicia will be exhibiting and lecturing at "Affärsutveckling för medicintekniska produkter 2020" in Stockholm. Join us for...

Thank you for this year, Arab Health!

We had four fantastic days with exciting meetings and networking,Arab Health - thank you for this year’s conference!

How to ensure maximum returns from investigation initiated studies

Sofia Nordgren, our Chief Compliance and Regulatory Officer (CCRO) and Director of Regulatory Affairs, was spreading the knowledge about how...