<H1> The UK MHRA Compliance Countdown Has Started for the Manufacturers of </H1> |
<H1> The Clock is Ticking!
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<H2> All Devices and IVDs Marketed in India Now Have to be Listed with SUGAM portal by </H2> |
<H2> Start Complying Today </H2> |
<H2> EU-based manufacturers now require a Swiss Agent for marketing new and existing devices in Switzerland adhering to transitional timelines </H2> |
<H2> Compliance Countdown </H2> |
<H2> Expedited Product Classification
and NIOSH Certification for N95 Respirator </H2> |
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with Offering Services in 120+ Countries and 600+ Global Clients </H2> |
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<H3> Have You Listed Your Devices Yet? </H3> |
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<H4> October 1, 2021 </H4> |
<H4> October 1, 2022 </H4> |
<H4> October 1, 2023 </H4> |
<H4> BlogS </H4> |
<H4> Case studies </H4> |
<H4> mandates </H4> |
<H5> Director, Regulatory Affairs, </H5> |
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<H5> Associate, Regulatory Affairs Team II, </H5> |
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<H5> We’re here to help and answer any question you might have.
We look forward to hearing from you. </H5> |
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