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๐ˆ๐ง๐๐ฎ๐ฌ๐ญ๐ซ๐ฒ ๐•๐จ๐ข๐œ๐ž๐ฌ: โ€œ๐„๐” ๐ซ๐ž๐ ๐ฎ๐ฅ๐š๐ญ๐ข๐จ๐ง๐ฌ ๐š๐ซ๐ž ๐œ๐ซ๐ฎ๐ฌ๐ก๐ข๐ง๐  ๐ข๐ง๐ง๐จ๐ฏ๐š๐ญ๐ข๐จ๐ง ๐ข๐ง ๐Œ๐ž๐๐“๐ž๐œ๐ก.โ€ Thatโ€™s not a hot take, itโ€™s the view from someone whoโ€™s been reporting on them since the beginning. We spoke with Amanda Maxwell, EU MedTech Regulatory Affairs Editor at Medtech Insight, to unpack whatโ€™s really going on behind the scenes. ๐Ÿšง Why start-ups are dropping outย  ๐Ÿ‡ฌ๐Ÿ‡ง What the UK is doing differentlyย  ๐Ÿ“‰ How regulation is shaking the marketย  ๐Ÿ‘€ And whatโ€™s coming next ๐Ÿ‘‰ If you work in MedTech, this is one to read: https://lnkd.in/dYqVMCvY ๐Ÿ‘‰Hey, you can also swap insights with our Critical specialist, just connect with Ana Rita: https://lnkd.in/d9E2i3Nvย  #CriticalSoftware #TheFutureIsOurs #SoftwareSolutions #DigitalTransformation #Technology #Tech #MedTech #MedicalDevices #DigitalHealth #MDR #IVDR #AIinHealthcare #RegulatoryAffairs #Brexit

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