.Dr. John Nkengasong today underscored PEPFAR’s deep commitment to addressing inequities for children impacted by #HIV at a Congressional briefing with Rep. Barbara Lee and sponsored by Elizabeth Glaser Pediatric AIDS Foundation and World Vision. #AIDSFreeGeneration

On 9/10, an FDA delegation met with members of Costa Rica's Global Life-Centered Hub to explore opportunities for regulatory harmonization, convergence, and reliance. Collaborative efforts like these are key to advancing and fostering innovation.

Today, FDA issued warning letters to two Chinese nonclinical testing laboratories, citing both for laboratory oversight failures and animal care violations that raise concerns about the quality and integrity of data generated by the labs. fda.gov/news-events/pr…

Yesterday in San Jose, FDA Global's Mark Abdoo and delegation met with Costa Rica’s Vice President and Minister of Health Dr. Mary Munive Angermiller & Ministerio de Salud de Costa Rica officials to discuss advancing regulatory harmonization and regulatory reliance in Central America and the Caribbean.

Welcome to India! Wishing the FDA Global FDA delegation of experts on generic drugs a productive week of engagement, learning, and meaningful exchanges. May your time here foster deeper collaborations and inspire impactful outcomes for patients everywhere. #IndiaEngagement

As we prepare for #UNGA79, read how conflict increases the spread of dangerous germs & learn more about CDC’s role in combating the threat in Rolling Stone’s article: bit.ly/3WeSP9u

India's Mepro Pharmaceuticals—with support from USAID's PQM+ Program—received approval from World Health Organization (WHO) for a treatment for 2 life-altering Neglected Tropical Diseases. This milestone enhances the global supply of a critical medicine! #BeatNTDs U.S. Pharmacopeia neglecteddiseases.gov/who-prequalifi…

Attending Science Summit UNGA? Check out 'Exploring novel solutions for tracking & adapting to the health impacts of climate change in resource-constrained settings,' a hybrid event featuring Fogarty's Brad Newsome. TOMORROW!! September 13 at 1:00 p.m. ET (USA). Organized by DS-I Africa

On October 8, 2024, from 1:00 -2:00 p.m. ET, the U.S. FDA will host a webinar on The Voluntary Improvement Program: How to Enroll, Opportunities, and Best Practices. FDA staff will answer questions related to the program. fda.gov/medical-device…

The latest CDC Antimicrobial Resistance comment in The Lancet highlights the growing threat of #AntimicrobialResistance and emphasizes why the #UNGA79 High-Level Meeting on #AMR this month is critical for sustained action on AMR not only in our countries but globally. 🌎🦠 #One Health

What is PMI REACH Malaria? Join us on Wednesday to meet REACH staff and learn more about our newest #malaria service delivery project! 🗓️ September 18 ⏰ 9:30am ET | 3:30pm CET | 4:30pm EAT 📱 Register: ow.ly/FG8e50T4agx

Today, we issued a draft guidance for industry that, when finalized, will provide sponsors with recommendations for conducting multiregional clinical trials in support of applications for drugs intended to treat cancer. fda.gov/news-events/pr…

The U.S. FDA welcomes the global community to the 26th session of the International Medical Device Regulators Forum (IMDRF) in Seattle. Learn more about #IMDRF: fda.gov/medical-device…

Happening TODAY at 1 pm ET (USA)! Department of State and CUGH symposium, 'Global Health Security: The Intersection of Policy and Academia.' Panelists include #Fogarty Director Kathleen Neuzil. Register: ow.ly/j9IT50TmQrh #GlobalHealth 🌍🔬🏥

Today is #WorldPatientSafetyDay.   A safe diagnosis requires the joint efforts frompatients, families, healthcare workers, and policy-makers.  Get it right; make it safe!   👉 paho.org/en/campaigns/w…    #HealthForAll

Reaching an accurate diagnosis is a complex process. Health workers can 🎓 Keep up with education & training, 🤝 Collaborate proactively with colleagues, 👥 Consider patients as part of a team, 🔎 Recognize biases, to get it right, make it safe 👉bit.ly/WPSD2024WHO

Couldn’t join us for the International Medical Device Regulators Forum (IMDRF) in Seattle? Here’s a recap of what you missed so far. Day 1 highlighted how harmonization, convergence, and reliance promote a more effective regulatory model for #MedicalDevices.

📣Join #CDERSBIA on Oct 16 to learn about how Identification of Medicinal Products (IDMP) offers a global framework for the unique identification and consistent documentation of medicinal products, facilitating effective information exchange. Register ➡️ fda.gov/drugs/news-eve…