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
Cervical cancer is something that every woman has to be concerned about. More common in women over the ...
One of the main reasons the Federal Food and Drug Administration issued warning letters to CBD ...
As 2021 has come to a close and companies are holding and finalizing their last management reviews, ...
Labeling for medical devices is under strict regulations. The requirements are dependent on the class ...
Developing a Design and Development Plan is a part of the design controls process required by the FDA ...
Manufacturers may find themselves without the resources and processes needed to effectively and ...
A Non-Conforming Material Report or NCMR is the standard way to report a material that does not meet the ...
On Friday, Proctor & Gamble announced a voluntary recall of several of their aerosol dry shampoo ...
When registering a medical device with the FDA the type of product influences the method of pre-market ...
The idea behind the management review process is to take a step back from the day-to-day operating of ...
One of the more ambiguous parts of the Quality System Regulations, 21 CFR 820, is making judgments ...
Registering a new device with the FDA can be tricky. The first step is to choose what pathway to follow ...
Ready to learn more about working with us?
