Surgeon General nominee Dr Casey Means, a confidante of HHS Secretary Robert F Kennedy, was grilled in a tense Senate confirmation hearing on Wednesday. She fielded questions on vaccines, her conflicts of interest, pesticides, and birth control, and reaffirmed her focus on America’s chronic disease epidemic, promising to use her platform to promote “whole healthy […] Continue reading ->
The US Health and Human Services (HHS) has cancelled this week’s meeting of its Advisory Committee on Immunization Practices (ACIP) amid a court challenge to the committee’s composition and decisions, led by the American Academy of Pediatrics (AAP). Meanwhile, the long-delayed Senate panel confirmation hearing for US President Donald Trump’s nominee for Surgeon General, Casey […] Continue reading ->
Every $1 invested in the Medicines for Malaria Venture (MMV) between 2000 and 2023 yielded $13 in monetised health benefits, according to a study published in The Lancet Global Health this week. MMV is a not-for-profit product development partnership (PDP) that works with public and private sector partners to discover, develop and deliver accessible and […] Continue reading ->
A dispute over technology transfer rights pushed the World Health Organization (WHO) to delay its Global Action Plan on Antimicrobial Resistance (AMR) for further informal talks. Instead, the Executive Board approved a compromise drafted by Nepal and Ethiopia on Wednesday to reopen negotiations on intellectual property, specifically regarding “voluntary and mutually agreed technology transfers.” This […] Continue reading ->
STRASBOURG – The European Parliament backed the EU’s Critical Medicines Act (CMA) on Tuesday in a decisive move to secure Europe’s pharmaceutical supply chains from geopolitical shocks. With an overwhelming majority of 503 votes in favour, 57 against, and 108 abstentions, MEPs endorsed a sweeping industrial policy designed to re-shore the production of active ingredients […] Continue reading ->
The European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) have jointly established new AI principles in drug development to reduce regulatory divergence between the major markets of the European Union and the United States. Industry associations have applauded the landmark accord, as it strengthens harmonisation across the regions – but emphasise […] Continue reading ->