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#2019RAPS on Twitter

RT @ClarivateHealth: Panelist: Developers should have as many interactions as possible w/ regulator for cell & gene therapies because of va…

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Some manufacturers are failing to grasp the step change in clinical and risk management requirements imposed by the EU's new Medical Devices Regulation, a panelist said at #RAPSConvergence 2021. Regulatory Focus explains: https://t.co/lHWF49yAYn

Regulatory Affairs Professionals Society

This year's #RAPSConvergence is in the books. “I really must applaud the efforts of everyone who made this year’s Convergence such a success,” said Convergence Planning Committee Chair Meg Mucha Couldn't agree more. https://t.co/CaoCBeoIZQ https://t.co/qoTaDqIteI

Regulatory Affairs Professionals Society