Blog2025-08-12T11:54:14-03:00
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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/ [...]

FIME 2017

Passarini Regulatory Affairs confirms presence of its consultants at FIME 2017 - medical fair in Orlando - USA. August 8-10, 2017 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 up with our [...]

Hospitalar Fair 2017

Hospitalar Fair 2017 Passarini Regulatory Affairs will be, for the first time, with a stand at the Hospitalar Fair to attend companies and talk with clients. May 16-19, 2017 Expo Center North Rua José Bernardo Pinto, 333 - Vila Guilherme - São Paulo / [...]

News in CE process

News in CE Process It was published today, May 5, 2017, the new Directive that regulates the medical devices replacing the Directive 93/42 / EEC EC. Click here to access in full the original text of the New Directive for CE mark. Do you have any [...]

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