Welcome to the team!
Welcome our newest rockstars to Key2Compliance, Heléne Lindegren, Malin Borg, Dalia Rhman och David Dahi. Four individuals who are joining us and no doubt will have a huge impact on their clients and teams! Welcome to the team! HELÉNE LINDEGREN, Business & Contract Manager What will be your role at Key2Compliance? My role at Key2Compliance […]
Meet our speakers at the Medical Device Product Life Cycle Conference!
We are excited and proud to have some of the most experienced speakers within the industry present at our Medical Device Product Life Cycle conference in Lund on the 26-27th of October. Become inspired, get the latest knowledge, and turn your compliance strategies into a tool for success! Meet our speakers: Erik Hansson, Senior Expert […]
Welcome our next speaker – Åse Ek!
Medical Device Product Life Cycle – a conference for QA & RA professionals! Let’s welcome our next speaker in line , Ase Ek, Senior Consultant and Trainer at Key2Compliance to our Medical Device Product Life Cycle conference!! 𝗕𝗲𝗶𝗻𝗴 𝘁𝗵𝗲 ‘𝗣𝗲𝗿𝘀𝗼𝗻 𝗥𝗲𝘀𝗽𝗼𝗻𝘀𝗶𝗯𝗹𝗲 𝗳𝗼𝗿 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲’ – 𝗶𝘀 𝘁𝗵𝗶𝘀 𝗶𝗻 𝗳𝗮𝗰𝘁 𝗮 𝗾𝘂𝗮𝗹𝗶𝘁𝘆 𝗰𝗼𝗻𝘁𝗿𝗼𝗹, 𝗿𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗮𝗳𝗳𝗮𝗶𝗿𝘀, 𝗼𝗿 […]
Meet Josef Smeds at our Medical Device Product Life Cycle Conference
Medical Device Product Life Cycle – a conference for QA & RA professionals! We are excited to welcome another speaker to our Medical Device Product Life Cycle Conference; Josef Smeds, Managing Director at NordicInfu Care AB How the industry work to meet both user needs, and expectations from the buyers This presentation will focus on the […]
The new version of Annex 1 is published, finally!
Key2Compliance has prepared for the publication for a long time and we have webinars, training courses and consultation services ready to support you. First out is a webinar together with the Danish Medicines Agency on October 11th. After that, we run a number of courses on Annex 1 and related subjects like Contamination Control Strategy […]
Speaker announcement: Sofia Segersson from Diabetesia
Medical Device Product Life Cycle – a conference for QA & RA professionals! We are happy to welcome the next speaker to our Medical Device Product Life Cycle – QA/RA conference on the 26-27th of October in Lund: Sofia Segersson, Owner, Consultant, Entrepeneur at Diabetesia.se Sofia will speak about a very interesting topic “Medical Devices as Part of […]
Speaker announcement: Judith de Wilde from Axon Lawyers
Make compliance your success factor – a conference for QA/RA professionals We are delighted to welcome the next speaker to our Medical Device Product Life Cycle – QA/RA conference on the 26-27th of October in Lund: Judith de Wilde, Attorney at Law at Axon Lawyers Judith will deliver two presentations at the conference: Interaction between manufacturers […]
A warm welcome to our two new team members!
We are glad to share with you that our Key2Compliance team has recently been joined by two new team members – Erik and Susanna. We are excited to introduce you to these two talented additions to our team! ERIK BOM, Medical Device QA/RA Consultant What will be your role at Key2Compliance? I will work as […]
Inside Medicon Valley
Don’t miss the article about Key2Compliance in the new magazine “Inside Medicon Valley”. The article focuses on “The survival of devices following EU-MDR and FDAs more stringent scrutiny on clinical data”. Inside Medicon Valley is a new magazine, highlighting what’s happening in the Swedish-Danish life science region. Medicon Valley is the strongest life science cluster […]
First speaker announced – Medical Device Product Life Cycle Conference
Make compliance your success factor – a conference for QA/RA professionals We are delighted to introduce the first speaker Cyrille Michaud at our upcoming conference on the 26-27th of Ocotober in Lund, Sweden. The title of Cyrille’s presentation is “Device Software and Change control – how can SW manufacturers manage changes under MDR?” Short introduction […]