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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

July 2, 2024

Life Sciences’ Brazil Global Guide 2024 is now available

We are pleased to announce our collaboration on the Chambers and Partners Life Sciences 2024 Global Practice Guide! Our partners Priscila Kashiwabara Life Sciences’ Brazil Global Guide 2024 is now available

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May 29, 2024

New Regulation Approved by Anvisa Simplifies the Registration Process for Biosimilar Medicines

Anvisa approved the new simplified regulation for the registration of biosimilar medicines, whose publication in the Official Gazette (DOU) is still awaited. New Regulation Approved by Anvisa Simplifies the Registration Process for Biosimilar Medicines

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April 17, 2024

Anvisa opens its doors to Startups: Stepping towards Innovation in Medicines

Anvisa recently launched a public notice with the aim of selecting Startups involved in the research and development of medicines, in order Anvisa opens its doors to Startups: Stepping towards Innovation in Medicines

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