The work of Dr. Paul M. Zoll provided the foundation for ZOLL® Medical. Visit our website to find out more about us: https://bit.ly/3KNiXCQ And join the ZOLL community to stay in the know: https://bit.ly/3Vh79id #DiscoveringZOLL #ZOLLMedical
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Executive Regulatory and Quality Consultant & Trainer | MDR | IVDR | Combination Devices | Clinical | | Conformity Assessment Support
The EU #MDR is a never ending story which will keep us busy. We need to take a step back and ask ourselves why legislations are there. They are there to enable innovation and controlled market access and should never be a bottleneck. Let’s hope that all these measures would lead to reasonable and patient oriented measures soon!
Ensuring the supply of medical devices - strengthening the healthcare industry in the long term On Wednesday, June 5, a hearing was held in the German Bundestag on securing the supply of medical devices. Royth v. Hahn, Erik Vollebregt, and Christina Ziegenberg among others, commented on this topic. The hearing is in German. It and the statements can be viewed here: https://lnkd.in/eAt2zSsj #AstraCon #Bundestag #MDR #MedicalDevices
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Read our feature in the Albuquerque Journal highlighting our latest medical innovation that provides state-of-the-art advancements for both patients and providers in #NewMexico at https://bit.ly/3RRiqnz.
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𝗪𝗶𝘀𝗱𝗼𝗺 𝗪𝗲𝗱𝗻𝗲𝘀𝗱𝗮𝘆 Remember that in the medical device field, innovation should be driven by real world clinical needs and patient outcomes, not just by technological possibilities. How do you ensure that innovation in the medical device industry remains focused on addressing real-world clinical needs and improving patient outcomes? Share your strategies or thoughts below! #WisdomWednesday, #MedicalDeviceInnovation, #ClinicalNeeds, #PatientOutcomes, #TechnologyInnovation, #HealthcareInnovation, #IndustryInsights, #PatientCenteredCare, #InnovationStrategy, #ProfessionalDevelopment
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The right engagement will bend the medical cost trend of an organization. Download the whitepaper to find out how.
Consultants, bend your clients' medical cost trends by helping them engage their employees early. Download our whitepaper to find out how: https://lnkd.in/ePYm2hkZ
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◆ Empowering Medical Device Professionals to Move from Standing Still to Climbing the Corporate Ladder◆ Executive Coach & President◆ Past President & CEO Radi Medical Systems ◆ Author of Motivation Now! ◆ MedDevCoach.com
𝗪𝗶𝘀𝗱𝗼𝗺 𝗪𝗲𝗱𝗻𝗲𝘀𝗱𝗮𝘆 Remember that in the medical device field, innovation should be driven by real world clinical needs and patient outcomes, not just by technological possibilities. How do you ensure that innovation in the medical device industry remains focused on addressing real-world clinical needs and improving patient outcomes? Share your strategies or thoughts below! #WisdomWednesday, #MedicalDeviceInnovation, #ClinicalNeeds, #PatientOutcomes, #TechnologyInnovation, #HealthcareInnovation, #IndustryInsights, #PatientCenteredCare, #InnovationStrategy, #ProfessionalDevelopment
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A lot of medical data is created every day, but it is not managed productively. This calls for more effective healthcare management, as inappropriate referrals and rising administrative costs create financial pitfalls. Compared to traditional medical devices, the MESI mTABLET platform provides a holistic approach to medical assessment, turning data into information and helping physicians make informed decisions in less time. For more information on which measurements are supported, click here: https://hubs.ly/Q02qHt_P0. #MESImTABLET #innovationinhealthcare
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OB/GYN's, should not: - Let their patients go elsewhere - Ignore the power of medical devices - Keep a fixed mindset on what they can & cannot offer Instead, they should expand their practise. Step 1: Buy a medical device to fix all concerns we addressed. - ✅My suggestion: 🟢https://lnkd.in/gZ_Pd34q
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That's great to see that Health Canada | Santé Canada recognized ✅ ISO 10993-23 Tests for irritation (partly) ✅ ISO 11737-3 Bacterial endotoxin testing (fully) For ISO 10993-23 the following sections are NOT recognized: 📍 Clause 4 General principles – Step-wise approach 📍 Clause 6 In vitro irritation tests 📍 Annex B Test method checklist for in vitro irritation testing using reconstructed human epidermis models 📍 Annex C Example of method documentation sheet for reconstructed human epidermis models And there are several updates related to 📌 ISO 10993-3 Tests for genotoxicity, carcinogenicity and reproductive toxicity 📌 ISO 10993-10 Tests for skin sensitization 📌 ISO 10993-13 Tests for local effects after implantation 📌 ANSI Z80.7 Ophthalmic optics – Intraocular lenses Stay updated!
Health Canada has updated its list of required standards for medical device. It is important for companies to review the list to ensure they have applied the most current versions of the standards. https://lnkd.in/gd7h-JvQ #healthcanada #listofstandards #medicaldevice
Draft list of recognized standards for medical devices
canada.ca
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Health Technology Assessment (HTA) has been around for over 50 years, yet there is still significant room for improvement in its application, especially when it comes to technologies other than pharmaceuticals, such as medical devices and digital medical devices. Let's discuss this further at the ISPOR Saudi Arabia on June 11th. #HealthTechnologyAssessment #MedicalDevices #DigitalHealth #ISPOR #healthpolicy #valuemeasurement Yazed AlRuthia Hussain Al-Omar SDA Bocconi Università Bocconi Carlo Federici Amelia Compagni
📢 Learn about the latest in HTA for Medical Devices with Dr. Rosanna Tarricone! 🏥🔬 Get insights on the evaluation and assessment of medical devices for optimal healthcare outcomes. 🗓️ 11th of June 🔗 Register now: https://lnkd.in/dyeAJzEk #ISPOR_Saudi24
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2moWell done!