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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.
Join us in Amsterdam on May 8 and 9 for a special volunteer opportunity to play a key role in bringing these certification programs to life. Travel and hotel expenses incurred by volunteers will be reimbursed by RAPS. If you have experience in regulatory compliance and a passion for the field, we'd love to hear from you. Preference will be given to applicants located in the EU but is not a requirement for selection.
This is a unique opportunity to be a part of something truly meaningful and make a positive impact on the regulatory compliance profession.
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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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