Standards and Regulations Workshop for startups in healthtech

Are you intending on bringing a medical device or life science innovation to the market to treat humans? Then our upcoming workshop on Thursday, June 6th, may be super relevant for you! 🔬✨ Join us on June 6th from 10:00 to 12:00 at UtrechtInc's Learning Space for a workshop on 'Standards and Regulations' for startups in healthtech, hosted by experts from Qserve Group. If you're bringing a medical device or life science innovation to market, compliance with standards and regulations is crucial. In this session, the experts of Qserve guide you on navigating this complex landscape, including where to find regulations, what they mean for your company and device, and when to start with documentation. 📝🔍 Key topics we'll cover: 👉 Regulatory, quality, and clinical affairs: understanding their implications. 👉 Essential information needed for product approval. 👉 Timing considerations for documentation commencement. This interactive session offers you the chance to ask questions and engage with fellow participants. Plus, following the workshop, you'll have the opportunity for one-on-one discussions with their experts to gain valuable insights and advice. 💬💡 No need to sign up, just drop by at UtrechtInc on June 6th at 10:00. See you there! 👋

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