Good morning everyone, I'm hoping Friday morning is a good time to request 10 minutes of your time to complete my thesis ...
📣📣 Calling all Medical Device Professionals of LinkedIn who are implementing the EU MDR and watching out for the UK MDR📣📣 ...
Thanks to everyone who contributed to the information on training Institutes in Ireland. The details are now listed in the RAPS ...
Hi Bernie I am sure they have. Due to audit here in Oct, so am sure we are not the first. Regards ...
Hi Martin My experience has been regulators will accept the timeline you establish as long as the logic is sound and ...
Has the HPRA audited any Irish manufacturing site since MDR came into force? Le meas, Bernie ...
Hi, interested to find out common approach to establishing CAPA timelines where regulatory approvals (FDA, NB etc.) are required ...
https://www.iqc.ie/training/ Irish Quality Centre deliver public and private training for Medical Device including (but ...
Hi Edward Apologies for delay – is a hectic time! I have completed the questionnaire – wishing you the best of luck. ...
Good morning all, TGIF :) As part of the masters in reg affairs and need to do interviews and a survey to support the ...
Overview: This webinar focuses on unfolding opportunities for different key stakeholders to fully understand ...
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