Our calendar informs on industry events, upcoming compliance deadlines, as well as new Obelis webinars.
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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 (high-risk IVDs that were self-certified under IVDD but now require a… |
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