Healthcare Quality Improvement Partnership (HQIP)’s Post

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Pharmacist and Medical team both for patients: Time to Reperfusion, Door-to-Balloon Times, and How to Reduce Them A very important medical intervention to be performed in patients. Time to reperfusion and first-medical-contact-to-balloon times are key parameters in assessing efficiency of the primary PCI pathway while also being powerful predictors of outcome. This chapter discusses the role of these measures and how improvements may impact clinical outcomes. I am sharing below some key information to summarize it https://lnkd.in/gzc5DCzx

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I'll be speaking at the 3rd conference on Clinical Studies with Medical Devices and IVDs on some of the pitfalls within emergency studies and how to work with studies without any obvious benefit. The conference will take place in London on May 29-30. I hope to see you all there. Experts will lead discussion panels. Registre here: https://csmd2024.com/ Chaired by Helene Quie Professor Brian D Smith Esther Gerteis Anette Kristiansen Sumit Mehta Ciska Janssens-Böcker Hindrik Robbe Marika Chrápavá Naeem Noordin Maria Nyåkern Daniela Giroud Eva Dahlberg Benjamin Joas Rieck Carlos Galamba Cécile van der Heijden Frank Rademakers Amie Smirthwaite, PhD, FRAPS and Simon Lidgate #medicaldevice #medicaldevices #clinicalstudies #ivd #clinicalresearch #clinicaltrials #regulatoryrequirements #regulatorycompliance #medicaldeviceregulation #regulations #biovents #MDR #IVD #regulatoryaffairs #acutestudies #benefitrisk

Register & Save! The 3rd Conference on Clinical Studies with Medical Devices and IVDs #CSMD2024 📅 29-30 May 2024 📌 London, UK Chaired by Helene Quie #medicaldevice #medicaldevices #clinicalstudies #ivd #clinicalresearch #clinicaltrials #regulatoryrequirements #regulatorycompliance 

If you’re conducting a clinical investigation in an EU Member State, you are required to submit a clinical investigation report (CIR) along with a summary of the CIR to that Member State. So far there hasn't been any guidance, but it's finally here. The Medical Device Coordination Group released Guidance (2023/C 163/06) “on the content and structure of the summary of the clinical investigation report”. Here’s what it has to say about what to include in the CIR summary. >> https://bit.ly/3RE4XzZ #clinicalinvestigation #clinicalinvestigationreport #eumdr #mdcg #medicaldevices #medtech

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Large, prospective, interventional clinical trials require significant funding and years of development and study execution before practice-informing results are available. There are many critical clinical questions that will never be addressed or addressable through prospective, interventional clinical trials. Criterium creates configurable electronic data collection tools for efficiently capturing retrospective data that will be submitted for subsequent analysis to answer clinical queries. Read our chart review case study: https://lnkd.in/gHvryvr #casestudy #clinicaltrials

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