Public Consultation on the Revision of RDC 327/2019: Main Changes and Criticisms
On March 26, 2025, the public consultation on the revision of RDC 327/2019, which regulates the health authorization, manufacture, import, marketing, prescription and inspection of cannabis-based products for medicinal purposes in Brazil, was approved.
Decree-Law No. 23/2025: New Rules for Cosmetic Products in Portugal
Decree-Law no. 23/2025 has been published, ensuring the implementation of Regulation (EC) no. 1223/2009 on cosmetic products. The decree comes into force on March 24, 2025 and establishes new rules to guarantee the safety of cosmetics on the Portuguese market.
Anvisa Returns to Publishing Medical Device Price Monitoring Data
Anvisa (the National Health Surveillance Agency) has announced the resumption of the publication of medical device price monitoring data in its Business Intelligence (BI) panels. The activity, which had been temporarily suspended, is now back, with improvements to the process and guarantees of greater efficiency and precision.