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SELECTBIO Conferences Point-of-Care Diagnostics & Global Health World Congress

James Boiani's Biography



James Boiani, Partner, Epstein Becker & Green, P.C.

James A. Boiani, MS, JD is a Partner in the Healthcare and Life Sciences Practice of Epstein Becker & Green, P.C., where he helps clients navigate complex issues associated with the regulation in vitro diagnostics and other medical devices, drugs, biologicals, combination products, and laboratory developed tests. He has helped clients navigate FDA challenges during product development (e.g., negotiating trial design issues with FDA), the regulatory review process (e.g., 510(k), CLIA waiver, and NDA reviews) and associated regulatory strategies, and in post-market compliance matters (e.g., quality systems, product recalls and regulatory reports, import issues, advertising and promotion). He also counsels testing services providers and a variety of investors with an interest in the life sciences. Mr. Boiani also is the Founder and General Counsel of the Coalition for CLIA Waiver Reform, an organization that has successfully advocated for changes in FDA policies that will improve access to safe, effective, and innovative waived testing for patients at pharmacies, clinics, urgent care centers, and physician offices. Prior to entering the legal profession, James earned degrees in chemistry from MIT and Cornell University, and worked as an environmental consultant on chemistry and regulatory issues, including development and U.S. EPA approval of industry-developed tests for water quality.

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Regulatory Briefing: Overcoming Regulatory Challenges in Bringing Point-of-Care Tests to Market

Monday, 28 September 2015 at 13:30

Add to Calendar ▼2015-09-28 13:30:002015-09-28 14:30:00Europe/LondonRegulatory Briefing: Overcoming Regulatory Challenges in Bringing Point-of-Care Tests to MarketPoint-of-Care Diagnostics and Global Health World Congress in San Diego, California, USASan Diego, California, USASELECTBIOenquiries@selectbiosciences.com

Point-of-Care Testing has had a profound impact on patient care, and the public health benefits of expanding access to more novel POCTs is
unquestionable.  However, going through the FDA review process to get the marketing clearances and approvals you need to take tests from the bench
top to the bedside is no easy task.  In this presentation, we'll explore strategies to prevent and solve obstacles arising during FDA pre-market and CLIA Waiver reviews.


Add to Calendar ▼2015-09-28 00:00:002015-09-30 00:00:00Europe/LondonPoint-of-Care Diagnostics and Global Health World CongressPoint-of-Care Diagnostics and Global Health World Congress in San Diego, California, USASan Diego, California, USASELECTBIOenquiries@selectbiosciences.com