Blog2025-08-12T11:54:14-03:00
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Health Product Labeling Information

Health Product Labeling Information There has been increasing demand for questions about the correct interpretation of the label content of single-use products available on the market. For a better understanding about it, ANVISA published on October 3, 2013, a technical note clarifying and detailing the [...]

Promo – August in Double

August in Double Check below the promotion that will stir your month of August. Get 02 ANVISA REGISTRATION PROCESSES and pay only one. Send you requeriments to contato@passarini.com.br and get your quotation. Rules: The second application must be done until December 14th, 2018 and must [...]

FIME 2018

FIME 2018 Passarini Regulatory Affairs confirms presence of its consultants at FIME 2018 - medical fair in Orlando - USA. July 17-19, 2018 Location: Orange County Convention Center, Orlando - Florida Schedule a meeting by email: contact.usa@passarini.com.br Learn more about the event: https://www.fimeshow.com/en/home.html  Keep [...]

Brazil’s ANVISA Streamlines Medical Device Importation Processes

Brazil’s ANVISA Streamlines Medical Device Importation Processes A new ANVISA resolution has simplified medical device importation requirements for Brazil. Imported devices no longer have to undergo inspections at Brazilian points of entry. Additional changes to simplify ANVISA importation requirements are anticipated in the near future. [...]

Trade Fair Medica 2017

Trade Fair Medica 2017 Passarini Regulatory Affairs confirms presence of its consultants at MEDICA 2017 - medical fair in Düsseldorf - Germany. November 13-16, 2017 Location: Exhibition Centre and Congress Center, Düsseldorf, Germany Schedule a meeting by email: contact.usa@passarini.com.br Learn more about the event: https://www.medica-tradefair.com/ [...]

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