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RAPS is seeking volunteers with Medical Devices and In Vitro Diagnostics regulatory compliance experience to help develop upcoming certification programs. The creation of the PRRC role was a catalyst for developing these new certifications. The PRRC role was mandated in Article 15 of the EU MDR and EU IVD regulations. As a volunteer, you will have the opportunity to help shape the future of the profession and gain valuable insight and networking opportunities with peers.
Volunteers will meet several times virtually to produce exam questions. If assignment is completed in full, volunteers will receive a voucher to test for free in a future window.
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Leeann Manlove
Regulatory Affairs Professionals Society (RAPS)5635 Fishers Lane, Suite 400Rockville, Maryland 20852
raps@raps.org+1 301 770 2920
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