Post by Elos Medtech

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๐—–๐—ผ๐˜‚๐—น๐—ฑ ๐—ฝ๐—ฎ๐—ฐ๐—ธ๐—ฎ๐—ด๐—ถ๐—ป๐—ด ๐—ฏ๐—ฒ ๐˜๐—ต๐—ฒ ๐—ต๐—ถ๐—ฑ๐—ฑ๐—ฒ๐—ป ๐—ฏ๐—ผ๐˜๐˜๐—น๐—ฒ๐—ป๐—ฒ๐—ฐ๐—ธ ๐—ถ๐—ป ๐˜†๐—ผ๐˜‚๐—ฟ ๐—ป๐—ฒ๐˜…๐˜ ๐—น๐—ฎ๐˜‚๐—ป๐—ฐ๐—ต? Missed requirements, late-stage redesigns, shelf-life concerns, or failed validations can stall approvals and delay market entry. Without proactive planning, packaging can quickly become a weak link in an otherwise strong product story. Thatโ€™s why weโ€™re dedicating the first episode of ๐— ๐—ฒ๐—ฑ๐—ง๐—ฒ๐—ฐ๐—ต ๐— ๐—ถ๐—ป๐—ฑ๐˜€๐—ต๐—ฎ๐—ฟ๐—ฒ - our new Elos Medtech podcast series - to sterile packaging. MedTech Mindshare is a forum where leading experts meet to discuss the trends shaping innovation in medical device manufacturing. ๐—˜๐—ฝ๐—ถ๐˜€๐—ผ๐—ฑ๐—ฒ ๐Ÿญ: ๐—จ๐—ป๐—ฝ๐—ฎ๐—ฐ๐—ธ๐—ถ๐—ป๐—ด ๐—–๐—ผ๐—บ๐—ฝ๐—น๐—ถ๐—ฎ๐—ป๐—ฐ๐—ฒ "Regulatory requirements in sterilisation and packaging for new product launches" Host: Jodie Gilmore, CMO Elos Medtech Guests: Monica Burt CEO at MB&A & Sofie Hรถchstetter VP Sterile Solutions Elos Medtech Weโ€™ll explore: โ–ช๏ธ How regulatory shifts are reshaping packaging requirements โ–ช๏ธ Why early packaging integration in R&D helps avoid costly setbacks โ–ช๏ธ How innovations like coatings, complex geometries, or sharper edges are pushing sterile packaging to its limits And this is just the beginning. Future episodes of MedTech Mindshare will dive into other critical questions driving medical device innovation, from manufacturing partnerships to R&D breakthroughs. Register today and be part of the conversation.