Blog2025-08-12T11:54:14-03:00
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RDC 982/2025: What’s Changing for the Good Practice Certificate?

ANVISA Publishes RDC 982/2025: Understanding the Optimization of Risk Management and Compliance Monitoring Keeping up with constant regulatory updates is essential for any company in the sector. The Passarini Group highlights the recent publication of ANVISA's Collegiate Board Resolution (RDC) No. 982, from July 28, [...]

Argentina’s Economic Revolution and the Medical Device Boom

Argentina: A Giant Awakens for the Medical Device Sector Argentina, a country that has historically navigated turbulent waters, now displays a promising horizon, flashing a green light for investors and companies, especially in the healthcare sector. After years of instability, the neighboring country shows robust [...]

Anvisa: Public Consultation on UDI for Medical Devices

Anvisa Opens Public Consultation on UDI: Understand the New Requirements for Medical Devices The Brazilian Health Regulatory Agency (Anvisa) has announced the opening of a public consultation to gather contributions regarding the requirements for the transmission and management of the Brazilian Unique Device Identification (UDI) [...]

ANVISA: A Complete Guide to Product Regulation in Brazil

Navigating the World of ANVISA with Passarini Group You might think dealing with ANVISA is a Herculean task, an insurmountable mountain of bureaucracy that drains your company's time and resources. But the truth is that ANVISA, as a health protection agency, ensures the safety of [...]

CE Marking as Your Passport to Success

Conquer the European Market with Passarini Group: CE Marking as Your Passport to Success The European market presents a promising opportunity for Brazilian companies seeking to expand their business, especially in the innovative medical products sector. While you may think that investing in CE certification [...]

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