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The Brazilian Health Regulatory Agency (Anvisa) will be present at the 46th meeting of the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH). The event took place in Vancouver, Canada, from June 9th to 14th.

With 17 representatives, designated by the Council’s guidelines and Ordinance 1,520/2019, which establishes the regulatory action model for the incorporation of topics transmitted by the ICH, Anvisa will participate in the meetings of the assembly, the management committee, and 14 working groups. Meetings take place simultaneously, seeking to discuss scientific and technical aspects of the development and registration of pharmaceutical products.

In addition, the Agency will send another three representatives to participate in specific working group meetings, which will take place in Berlin, Germany, from June 12th to 16th.

Parallel to the ICH meetings, the meeting of the International Pharmaceutical Regulators Program (IPRP) will be held, which exclusively brings together regulatory authorities. This meeting aims to promote cooperation and the exchange of information on matters of mutual interest.

Currently, Anvisa occupies the vice-presidency of the IPRP Management Committee and participates in 27 working groups related to the ICH, counting on the expertise of 50 specialists.

The ICH is an initiative involving regulatory authorities and the pharmaceutical industry, aimed at discussing and harmonizing scientific and technical aspects related to the development and registration of pharmaceutical products. In addition to Brazil, the regulatory authorities of the European Union, the United States, Japan, Canada, Switzerland, Mexico, Singapore, South Korea, China, Saudi Arabia, Chinese Taipei, and Turkey are also part of the program.


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