List of Contributions

Join the RAPS San Francisco Bay Area chapter for a full day of regulatory sessions related to the EU parliament’s latest decisions on the future of medical devices regulations in Europe, the EU commission’s recommendation and guidelines on unannounced visits and key requirements critical to demonstrating ...

Are you planning to take the US Regulatory Affairs Certification (RAC) exam this fall? If so, the RAPS San Francisco Chapter invites you to participate in a series of peer-led study sessions to help you prepare for the certification exam. This four-month program includes a series of four sessions—each ...

Join your regulatory colleagues from the San Francisco Bay area for the 21st annual FDA Pacific Region Update. This year’s full-day program includes an interactive session on FDA’s Case for Quality Initiative, led by representatives from the Center for Devices and Radiological Health (CDRH). This workshop ...

Join your quality and regulatory colleagues from ASQ Northern California Biomedical and the RAPS San Francisco Bay Area Chapter for a lively and informative one-day workshop addressing the best practices and lessons learned for successfully managing complex quality assurance and regulatory affairs ...

Medical Devices Easing 510(k) Process Involves Strategy, Learning About Competition, Meeting Told SANTA CLARA, Calif.--Regulatory affairs professionals need to be involved early on in a strategy for Food and Drug Administration submissions, including reaching out to marketing to learn what the ...