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By Giovanna Verginelli Mezher

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 and Viviane Trojan, along with attorneys at law Gustavo Vicenti and Giovanna Verginelli Mezher, authored the Life Sciences 2024 guide for Brazil, that outlines the regulatory framework for pharmaceuticals and medical devices, detailing the legislation, regulatory bodies and procedures for securing approvals and handling appeals. It covers categorisation, clinical trials, marketing authorizations and ongoing obligations.

The guide also emphasizes ANVISA’s role in regulation, the stringent requirements for biologics and the procedures for compassionate use and post-marketing surveillance. Additionally, it addresses manufacturing authorizations, distribution regulations and measures against counterfeit products.

For more details, click here.

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Last by Giovanna Verginelli Mezher

September 9, 2024

Brazil Implements a New Regulatory Framework for Food Products

The newly implemented regulatory framework governing food safety and quality in Brazil took effect on September 1st, 2024. The Collegiate Board Resolutions Brazil Implements a New Regulatory Framework for Food Products

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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

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