Stay updated about the latest events, webinars, and important deadlines.
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For in vitro diagnostic (IVD) manufacturers navigating the transition to the In Vitro Diagnostic Regulation (IVDR), a key deadline is approaching. The IVDR legacy extension applies only if manufacturers meet specific requirements: Submission of an application to a Notified Body ✅ Class D devices - by 26 May 2025 ✅ Class C devices - by… |
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Are Science and Beauty your work sectors? Then let's meet at NYSCC 2025, the premier event for personal care ingredients and formulations in North America! We are here to help your brand succeed in a globally regulated market.Why Meet Us at NYSCC?✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on… |
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Bringing Your Medical Devices to Market? Join us at FIME Miami, the largest international medical trade event in the USA!Our first goal? Supporting medical manufacturers in achieving regulatory compliance without the hassle. Why Meet Us at FIME? ✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory… |
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