Making Decisions in a COVID-19 World: Why Trusted Data Matters

Making Decisions in a COVID-19 World: Why Trusted Data Matters

  Mistake by Florida on child COVID-19 rate raises the question: Can Florida’s numbers be trusted?   “It’s unacceptable to publish information that changes so dramatically that it warrants explanation, and then to not provide any explanation,” said Jason Salemi,...
FDA Delays UDI Deadline for Class I Devices to September 2022

FDA Delays UDI Deadline for Class I Devices to September 2022

The US Food and Drug Administration (FDA) has released new guidance regarding Unique Device Identification (UDI) compliance dates for Class I and unclassified medical devices.  Effective immediately, the FDA has postponed GUDID (Global UDI Database) compliance for...

Innovit and atrify Renew Global Partnership

Global partnership will focus on providing customers with solutions to share reliable and proven product data with their business partners. SAN FRANCISCO – May 5, 2020 – PRLog — Innovit, a global software company specialising in UDI compliance...
EU-MDR Date of Application – Postponed…

EU-MDR Date of Application – Postponed…

The European Parliament has formally voted and adopted the amendment of its Medical Device Regulation (MDR) date of application. The Parliament has tabled and supported the 4 technical amendments proposed last week by the European Council, without bringing additional...
GUDID and UDI – Are You Prepared?

GUDID and UDI – Are You Prepared?

The Global Unique Device Identification Database (GUDID) is a database administered by the FDA that will serve as a reference catalogue for every medical device with an identifier. Unique Device Identification (UDI) is a system to mark and identify medical devices...