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By Giovanna Verginelli Mezher

Lexology GTDT – Pharma & Medical Device Regulation 2024

The chapter “Pharma & Medical Device Regulation,” authored by our partners Claudio Barbosa, Viviane Trojan and attorney at law Giovanna Mezher, has been published on the Lexology’s special guide, Getting The Deal Through.

The content covers a vast legislative material regarding the pharmaceutical and healthcare equipment sector in Brazil, delving into the regulatory framework, rules for clinical practice, marketing and amending authorizations, product recalls, advertising and promotion, off-label use and unlicensed products, as well as sale and supply regulations, along with updates and trends in the field.

On the website, you can find laws and regulations from countries around the globe in a democratized manner, available to everyone, with Kasznar Leonardos representing Brazil in this dissemination.

Read the full content here.

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Last by Giovanna Verginelli Mezher

4 de November de 2025

ANVISA Publishes New Proposal for Review of the Regulation on General Labeling of Packaged Foods: Public Consultation No. 1357/2025

The proposal for reviewing the regulation concerning the general labeling of packaged foods (including beverages, ingredients, additives, and processing aids) was published ANVISA Publishes New Proposal for Review of the Regulation on General Labeling of Packaged Foods: Public Consultation No. 1357/2025

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29 de October de 2025

Lexology Panoramic: Pharma & Medical Device Regulation 2026

We are pleased to share the Brazil chapter of the Pharma & Medical Device Regulation Panoramic guide, authored by our partners Claudio Lexology Panoramic: Pharma & Medical Device Regulation 2026

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30 de July de 2025

Weekly Update for Intellectual Property in Health

On July 28th, 2025, the Official Gazette of the Union (DOU) published Ministerial Ordinance GM/MS No. 7,687, dated July 24, 2025, issued Weekly Update for Intellectual Property in Health

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