MedTech Intelligence

Information polarization affects public opinion and investors. As we approach upcoming elections in different countries, it is crucial to understand how these political events could significantly reshape the landscape for MedTech investments. In this article, Ashkan Eliasy outlines an approach to help investors navigate and understand the interplay of political climates, cultural norms, and healthcare policies without getting emotionally attached to them. It also emphasizes the importance of open dialogue, diversity, critical thinking, and cross-cultural collaborations to determine the true potential of #MedTech innovations. #medtechinvesting

🔍 𝐃𝐨 𝐲𝐨𝐮 𝐤𝐧𝐨𝐰 𝐭𝐡𝐞 𝐌𝐚𝐧𝐝𝐚𝐭𝐨𝐫𝐲 𝐂𝐫𝐢𝐭𝐞𝐫𝐢𝐚 𝐟𝐨𝐫 𝐏𝐨𝐬𝐭-𝐌𝐚𝐫𝐤𝐞𝐭 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐅𝐨𝐥𝐥𝐨𝐰-𝐔𝐩 (𝐏𝐌𝐂𝐅) 𝐮𝐧𝐝𝐞𝐫 𝐭𝐡𝐞 𝐄𝐔 𝐌𝐞𝐝𝐢𝐜𝐚𝐥 𝐃𝐞𝐯𝐢𝐜𝐞 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐢𝐨𝐧 (𝐄𝐔𝐌𝐃𝐑)?  🎥 In our comprehensive webinar hosted in partnership with @MTI, industry experts Parvathi Nambiar and Smridula Hariharan, delve into the essential criteria that necessitate PMCF, including scenarios involving novel technologies, devices used in high-risk populations, or where long-term safety and performance data are unclear. This in-depth session offers valuable insights into navigating these regulatory waters with confidence. 🌐 Access the full on-demand webinar and gain crucial knowledge to ensure compliance with the evolving EUMDR: https://lnkd.in/gbskJ7ff 𝐊𝐞𝐲 𝐇𝐢𝐠𝐡𝐥𝐢𝐠𝐡𝐭𝐬 𝐈𝐧𝐜𝐥𝐮𝐝𝐞:  ▶ Detailed exploration of scenarios that mandate PMCF, helping you identify when your device must comply.   ▶ Strategies for crafting effective PMCF plans that address regulatory requirements and ensure device safety and efficacy.   ▶ Cost-effective approaches to conducting PMCF, utilizing real-world data and existing resources for comprehensive oversight.   ▶ Expert advice on overcoming common PMCF planning and execution challenges, equipped with real-world examples and actionable tips. Embrace the expertise and tailored solutions from Celegence as you navigate the complexities of medical device regulations. Our team is ready to boost your strategic capabilities, ensuring you meet the demands of #medicaldeviceregulation and #EUMDRcompliance with ease. #medicaldevices #regulatoryaffairs #compliance #regulatorystrategy #EUregulation #medtech #webinars #healthcarecompliance #medicalregulation #EUpolicy #regulatoryinsights #clinicaldata #postmarketsurveillance #Celegence #medtech #PMCF #EUMDR  #MedicalDeviceRegulation #PostMarketSurveillance #MedicalDevices #RegulatoryAffairs #MedicalCompliance #MedTechInnovation #HealthcareRegulation #ClinicalDataManagement #MedicalDeviceCommunity #RegulatoryStrategy #MedicalSafety #ClinicalEvaluation #RegulatoryCompliance 

🔔 Impact of #AIAct on the medical and healthcare sector #MDR 🔔 Join the conversation today at 16:00 CET https://lnkd.in/e92RZ9Yq

Tomorrow! Don't miss the "Mastering Compliance: Essential Insights into PMS Documentation" webinar in partnership with Celegence. REGISTER NOW: https://lnkd.in/eYb94nqR 📅 Date: April 24, 2024 | 🕙 Time: 10:00 a.m. ET (US) Join us to take a deep-dive into the world of Post-Market Surveillance Documentation, uncovering strategies to ensure #compliance in the #medicaldevice industry. Don't miss out on this invaluable opportunity to expand your knowledge! #pms #postmarketsurveillance #medtech

Although 61% of decision-makers at healthcare organizations said their firms invested at least $100 million in digital transformation initiatives over the past year, 65% of those respondents said their firms have translated less than half of those investments into tangible business value. Sateesh Seetharamiah highlights the challenges of digital transformation and key threat to success. #medtech #digitaltransformation

Survey closes soon. Get your response counted with the hundreds of our Medical Device organizations and regulatory professional readers. Results shared in a June Industry Report from MedTechIntelligence.com. https://lnkd.in/e49Qt3VG #medicaldevicecompliance #medtechregulatoryintelligence #FDA #EUMDR Rich West Rick Biros Inga Hansen

An average inflation rate of 1.8% may help aliviate some MedTech & Health System pressures, but be prepared for other challenges… https://lnkd.in/egAgUy_Q HUB International

Join us in Washington DC on June 3-5 for the Medical Device Regulatory Intelligence Summit. Hear new ideas, see industry trend data, explore the latest tools, software, and technologies, and network with regulatory officials and industry leaders. https://lnkd.in/egZvmuY4 #medicaldevice #MedTechCompliance #RegulatoryIntelligence

The consent decree restricts the production and sale of new continuous positive airway pressure (CPAP) machines, bi-level positive airway pressure (BiPAP) machines and other devices at several Philips Respironics facilities in the U.S. until certain requirements are met.

How is your Medical Device regulatory intelligence and compliance strategy stacking up? Give us your feedback and watch for results at MedTechIntelligence.com Take the survey: https://lnkd.in/e49Qt3VG