Join our friends at MassMEDIC for their Regulatory Roundup on Nov. 13, designed to give RA, QA and C-level executives updates on the global and domestic regulatory issues facing the industry. The agenda includes a keynote and Q&A with the newly confirmed Director of the Center for Devices and Radiological Health at the FDA, Dr. Michelle Tarver, as well as comprehensive presentations by industry representatives and regulatory experts. A limited number of in-person tickets remain, which include meals, snacks and ample networking time. A virtual ticket option is also available. Save 10% with code PARTNER10.
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