Post by Elos Medtech
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๐๐ผ๐๐น๐ฑ ๐ฝ๐ฎ๐ฐ๐ธ๐ฎ๐ด๐ถ๐ป๐ด ๐ฏ๐ฒ ๐๐ต๐ฒ ๐ต๐ถ๐ฑ๐ฑ๐ฒ๐ป ๐ฏ๐ผ๐๐๐น๐ฒ๐ป๐ฒ๐ฐ๐ธ ๐ถ๐ป ๐๐ผ๐๐ฟ ๐ป๐ฒ๐ ๐ ๐น๐ฎ๐๐ป๐ฐ๐ต? 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. Thatโs why weโre dedicating the first episode of ๐ ๐ฒ๐ฑ๐ง๐ฒ๐ฐ๐ต ๐ ๐ถ๐ป๐ฑ๐๐ต๐ฎ๐ฟ๐ฒ - 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. ๐๐ฝ๐ถ๐๐ผ๐ฑ๐ฒ ๐ญ: ๐จ๐ป๐ฝ๐ฎ๐ฐ๐ธ๐ถ๐ป๐ด ๐๐ผ๐บ๐ฝ๐น๐ถ๐ฎ๐ป๐ฐ๐ฒ "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 Weโll explore: โช๏ธ How regulatory shifts are reshaping packaging requirements โช๏ธ Why early packaging integration in R&D helps avoid costly setbacks โช๏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.