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India’s Pharmacopoeia Commission strengthened Northeast pharmacovigilance via new Nagaland partnerships, boosting drug safety and reporting.
Union Health Minister JP Nadda reviewed the Indian Pharmacopoeia Commission’s progress on December 26, 2025, highlighting improvements in medicine quality, safety, and regulatory standards.
The IPC, based in Ghaziabad, signed three new memoranda with Nagaland agencies to strengthen pharmacovigilance, expand adverse drug reaction reporting, and promote safe medicine use through the National Formulary of India—marking its first collaboration in India’s Northeast.
This follows the September launch of National Pharmacovigilance Week, which encouraged digital reporting of adverse reactions by healthcare providers and patients, supporting India’s push for scientific self-reliance and global pharmaceutical credibility.
La Comisión de la Farmacopea de la India fortaleció la farmacovigilancia en el noreste a través de nuevas asociaciones con Nagaland, impulsando la seguridad de los medicamentos y la presentación de informes.