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
As technology advances, more and more medical devices are being engineered with multiple functions. According to ...
Currently, we live in a world driven by the 4th Industrial Revolution in which science and technology are ...
The EU Compliance and Enforcement Group (COEN) recently released a new guidance document that provides information ...
I think I can speak for most people when I say that viable treatments and vaccines are desperately needed at this ...
In recent years, the field of regenerative medicine has gained significant traction and been pointed to as the ...
The US Food and Drug Administration released a final rule to exempt additional product codes from the requirements ...
A rising trend in the medical and computer science industries is Cloud Computing, or what is commonly known ...
The International Medical Device Regulators Forum (IMDRF) has recently issued a final guidance document to outline ...
Back in May, the FDA announced its intention to re-start domestic routine inspections (which you can read more ...
The EU Commission committed to provide information on the availability and the capacity of the notified bodies to ...
The medical device industry is constantly looking for innovative new ways to treat and cure conditions. Last ...
The UDI Rule requires a device to bear a UDI on its label and packages. Special labeling requirements apply to ...
Ready to learn more about working with us?
