Recent changes
Security Council Sanctions Committee Update
The UN Security Council Sanctions Committee provided an update on its sanctions list on March 10, 2026. This notice details amendments and additions to the list of individuals and entities subject to sanctions under Resolution 1988.
Security Council Removes Entry from Sanctions List
The UN Security Council's 1518 Sanctions Committee has removed one entry from its sanctions list. This action follows a review of listed individuals or entities subject to sanctions measures.
2026 Healthcare Trends: AI, Medical Device Cybersecurity, Digital Therapeutics
The IEEE Standards Association has identified key healthcare and life sciences trends for 2026, focusing on AI-driven health delivery, medical device cybersecurity, and digital therapeutics. The notice highlights opportunities and challenges associated with these evolving technologies.
IEEE Medical Device Registry Enhances Healthcare Cybersecurity
The IEEE Standards Association has launched the IEEE Medical Device Registry, a public database of medical devices that have successfully completed cybersecurity certification under the IEEE 2621 framework. This initiative aims to enhance transparency and trust in healthcare by providing verifiable information on device cybersecurity performance.
AI, 5G, Cybersecurity, and Data Interoperability in Connectivity
The IEEE Standards Association (IEEE SA) published a blog post discussing the future of connectivity, focusing on the integration of AI, 5G, cybersecurity, and data interoperability into intelligent infrastructure. The post highlights the evolving trends and the importance of consensus-based standards in shaping these advancements.
WHO Expert Committee on Biological Standardization Eightieth Report
The World Health Organization has published the eightieth report of its Expert Committee on Biological Standardization. This report details the proceedings and recommendations from the committee's meeting held in October 2024, focusing on the norms and standards for biological products.
WHO Expert Committee on Pharmaceutical Preparations Meeting
The World Health Organization (WHO) announced the Sixtieth meeting of the Expert Committee on Specifications for Pharmaceutical Preparations, scheduled for October 12-16, 2026. This committee advises the Director-General on medicine quality assurance and the maintenance of The International Pharmacopoeia.
WHO Expert Committee Adopts New Pharmaceutical Guidance
The WHO Expert Committee on Specifications for Pharmaceutical Preparations has adopted nine new guidance texts aimed at ensuring the quality assurance of medicines. These texts cover areas such as nitrosamine prevention, good manufacturing practices for excipients, and bioequivalence assessments, and are recommended for implementation.
WHO Expert Committee on Specifications for Pharmaceutical Preparations 57th Report
The WHO Expert Committee on Specifications for Pharmaceutical Preparations has released its 57th report, recommending new and revised guidance texts for pharmaceutical quality assurance. These include updated GMP for excipients, new GMP for radiopharmaceutical cold kits, revised lab quality control practices, and updated biowaiver guidelines.
Public Consultations on Drug Development Guidelines
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is seeking public input on proposed guidelines related to drug development standards. This consultation aims to gather feedback on new and revised guidelines before their finalization.
Get daily alerts for International
Daily digest delivered to your inbox.
Free. Unsubscribe anytime.
32 changes in last 7 days
Latest high priority updates
33 official sources tracked
Frequently asked questions
What does GovPing track in International?
33 official sources including government agencies, regulators, and courts. New rules, enforcement actions, guidance updates, and policy changes.
How quickly are changes detected?
Most sources are checked every 6-12 hours. Changes are classified by urgency and available within hours of publication.
Is GovPing free?
Yes. All data is free to browse, search, and subscribe to. GovPing is powered by Changeflow for teams that need more.
Can I get email alerts?
Yes. Subscribe to any combination of country, category, or role and get a daily digest of relevant changes delivered to your inbox.
What types of changes are classified as urgent?
Enforcement actions with penalties, rules with near-term compliance deadlines, product recalls, and binding rules that create new obligations for an entire industry.
Is there an RSS feed?
Yes. Every country, category, and source page has an RSS feed. Use it with any RSS reader for real-time updates without email.
Get International alerts
We'll email you when regulatory changes in International.