Resource Center
Find the latest content and resources from our team of experts to keep you in the know for all things quality and regulatory in the life science industry.
Sort by topic
Sort by resource type
Now more than ever, the Emergency Use Authorization (EUA) pathway for medical devices has become a popular topic. ...
The US FDA’s Center for Devices and Radiological Health (CDRH) announced a new pilot program that will allow the ...
In this webinar, we will be covering what exactly an SaMDs, or Software as a Medical Device, and go over some ...
In this second part of the webinar, we will review how to tackle changes that were made to the software post ...
This webinar will explore the Medical Device Single Audit Program, or MDSAP. We will provide an overview of the ...
One of the paradigms of the next generation computing tools is Augmented Reality (AR) where animated objects are ...
Few people outside of the industry know how big of a role the FDA has in product labeling and packaging. Every ...
The De Novo pathway establishes new classification categories for novel low-to-moderate risk devices, which in ...
Imagine a platform where innovations meet modern healthcare services while following regulatory requirements. Such ...
FDA recently released a proposed rule that amends its existing regulations around establishing the intended use of ...
One of the major pillars of the current Industry 4.0 is Automation. Indeed, technology is intervening in almost ...
Programmable Logic Controllers (PLCs) are the components that are used for interfacing between multiple hardware ...
Ready to learn more about working with us?
