A look at IP litigation in 2019 and the year ahead, and some advice on how medical device companies can safeguard their intellectual property.
This online series of workshops will arm you with the information you need to overcome challenges and achieve compliance with EU MDR.
Designers and manufacturers of both devices and software must conduct due diligence and ensure regulatory compliance in protecting user data.
The goal is to establish a baseline of cybersecurity hygiene and assurance for devices that are part of the national critical infrastructure software supply chain.
How will you make your company more attractive to investors?
When implementing IVDR requirements, it’s important to take a step back and look at the flow of documents.
The agency recently released a guidance document that gives device manufacturers an optional pathway to make certain modifications to their device.
The hot issues are related to compliance, EU MDR and recalls.
Technology will continue to evolve to allow patients greater control over their healthcare.
The idea of harnessing the body’s response to heal and defend is no longer the stuff of science fiction.