European Commission Presents Critical Medicines Act

European Commission Presents Critical Medicines Act

On March 12, 2025, the European Commission took an important step in strengthening the European Union's strategic autonomy with regard to the availability of essential medicines. It presented the Critical Medicines Act, a new initiative aimed at guaranteeing continuous access to essential medicines, preventing shortages and improving the resilience of supply chains in the pharmaceutical industry.

By |2025-03-21T10:20:33+00:0021 de March, 2025|brazil, ELS Group, General, Geral, Notícias, regulations|0 Comments

ANVISA Resolution No. 964/2025 published: Requirements for Forced Degradation Studies on Medicines

ANVISA Resolution No. 964 was published in the Federal Official Gazette (DOU) on February 24, 2025, establishing general requirements for conducting Forced Degradation Studies on medicines containing synthetic and semi-synthetic active pharmaceutical ingredients (APIs). The resolution also defines the parameters for the notification, identification and qualification of degradation products in these drugs. Below, we summarize the most important points of this new regulation.

By |2025-03-09T22:37:36+00:009 de March, 2025|ANVISA`, brazil, ELS Group, General, Geral, Notícias, regulations|0 Comments
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