MedTech

We are monitoring the ongoing developments with COVID-19 closely and following government and health organization guidelines. Our website provides the most up to date information on all our medical device events informaconnect.com/regulatory-aff…

Last chance! Early bird savings for #MedTech Summit 2022 end tonight. Book now to save £400: bit.ly/3se3l2R #EUMDR #MDR #EUIVDR #IVDR #MedicalDevices #Diagnostics #GlobalRegulations #Clinical #PMS #Law #Compliance #Software #AI #SaMD #ISO10993 #Biocompatibility

Last chance! Early bird savings for #MedTech Summit 2022 end tonight. Book now to save £400: bit.ly/3se3l2R #EUMDR #MDR #EUIVDR #IVDR #MedicalDevices #Diagnostics #GlobalRegulations #Clinical #PMS #Law #Compliance #Software #AI #SaMD #ISO10993 #Biocompatibility

Early bird savings for #MedTech Summit 2022 end midnight tomorrow! Book now to save £400: bit.ly/3se3l2R #EUMDR #MDR #EUIVDR #IVDR #MedicalDevices #Diagnostics #GlobalRegulations #Clinical #PMS #Law #Compliance #Software #AI #SaMD #ISO10993 #Biocompatibility

Early bird savings for #MedTech Summit 2022 end midnight tomorrow! Book now to save £400: bit.ly/3se3l2R #EUMDR #MDR #EUIVDR #IVDR #MedicalDevices #Diagnostics #GlobalRegulations #Clinical #PMS #Law #Compliance #Software #AI #SaMD #ISO10993 #Biocompatibility

Early bird savings for #MedTech Summit 2022 end this Friday, 25th February! Book now to save £400: bit.ly/3se3l2R #EUMDR #MDR #EUIVDR #IVDR #MedicalDevices #Diagnostics #GlobalRegulations #Clinical #PMS #Law #Compliance #Software #AI #SaMD #ISO10993 #Biocompatibility

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

Where are the main challenges for #MDR Implementation seen from the #notifiedbody perspective? I am chairing the session at #Medtech Summit 2021 where we are getting very helpful information from Ella Helgeman and Curtis Riley. The key message - Respec…lnkd.in/ddBrzkqV

Happy to be with Catherine Holzmann from GMED on the #EUIVDR Session at MedTech Summit 2021. The key message is: Date of Application of the Regulation remains the 26 May 2022 Only the transitional provisions are under discussion The proposal of the EU…lnkd.in/dG2awwaR

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

MedTech Summit conducted a survey of medical device professionals on implementing EU MDR. This report explores the data, revealing unique insights into how organizations have fared with EU MDR and the biggest obstacles that still remain informa.turtl.co/story/report-i…

Don't miss your chance to join the @EU_Commission, 20+ #CompetentAuthority and #NotifiedBody representatives, and hundreds of leading industry experts on 18-22 October 2021 at the virtual #MedTech Summit. Book now to save: bit.ly/3neSZxx #EUMDR #IVDR #GlobalRegulations

Practical advice session: - Malaysia & Singapore regulations & classification programme - Manufacturer’s shortcuts to regulatory access & registration - AMDD & its interaction with individual country legislation Info: bit.ly/3sAksu7 #MedicalDevices #RegulatoryAffairs

❓ When is it relevant to conduct a decentralized investigation? ❓ What are the pros and cons of decentralized v. traditional investigations? Don’t miss this valuable session at the #MedTech Summit: spr.ly/6016ysj7Q #EUMDR #MedicalDevices #ClinicalEvaluations