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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

16 de April de 2025

Medicinal Cannabis Review: Public Consultation 1.316/2025 open

The Public Consultation (CP) No. 1.316/2025, which aims to initiate the review process of Collegiate Board Resolution (RDC) No. 327/2019 from the Medicinal Cannabis Review: Public Consultation 1.316/2025 open

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10 de April de 2025

Life Sciences Brazil Global Guide 2025 | Chambers & Partners

We are pleased to announce our collaboration on the Chambers and Partners Life Sciences 2025 Global Practice Guide! Our partners Priscila Kashiwabara Life Sciences Brazil Global Guide 2025 | Chambers & Partners

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27 de December de 2024

Bioinputs Law: A new regulatory framework for sustainable agriculture in Brazil

On December 24, 2024, Law No. 15,070 of December 23, 2024 (“Bioinputs Law”), which regulates the production, use, and commercialization of bioinputs Bioinputs Law: A new regulatory framework for sustainable agriculture in Brazil

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