E-DRUG: Submission: Free FDA webinar for regulators
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USAID's Promoting the Quality of Medicines Plus (PQM+) program, which is led by USP, has teamed up with the U.S. FDA to develop a free, three-day online conference, "Regulatory Best Practices for Global Access to Medicines, Including Anti-TB Medicines." Dr. Atul Gawande, Assistant Administrator for Global Health, will provide a keynote address.
This virtual conference is an important opportunity for regulators and USAID staff to learn directly from the FDA, the World Health Organization (WHO), and U.S. Pharmacopeia (USP) about:
* FDA drug approval pathways and application review, including for new and generic drugs;
* The role of the FDA in international regulatory harmonization;
* Collaboration among the FDA, WHO, and national regulatory authorities to support the drug approval process in LMICs; and
* The role of USAID's PQM+ program in strengthening regulatory systems in LMICs.
The conference will take place August 16-18, from 8:30 - 12:30pm EDT.
For more details, please see the USP-Global-2022-Agenda.pdf
sbiaevents.com
<https://sbiaevents.com/files2022/USP-Global-2022-Agenda.pdf>
Register today Regulatory Best Practices for Global Access to Medicines (adobeconnect.com)
<https://events-na12.adobeconnect.com/content/connect/c1/1315899612/en/events/event/shared/3110197186/event_registration.html?sco-id=5136384581&_charset_=utf-8>
Megan Meline
Senior Communications Manager
Promoting the Quality of Medicines Plus (PQM+) Program
U.S. Pharmacopeial Convention
12601 Twinbrook Parkway, Rockville, MD, 20852, USA
Megan Meline <megan.meline@USP.org>