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
Biocompatibility is one of the most critical performance studies that manufacturers need to perform as part of ...
In the work from home era, we all realized how important it is to digitize our important documents and what a ...
Happy National Women’s Health Week! In honor of this week bringing light to important women’s health issues, I ...
National Women’s health week is a week-long observance by the US Department of Health and Human Services’ Office ...
EMMA International is continuing to celebrate Women’s Health Week! While there are so many reasons Women’s Health ...
The EU Commission released a new guidance document clarifying the purpose of harmonized standards under the EU ...
Deciding how and when to conduct stability tests on your new drug can be challenging. Stability tests provide ...
With healthcare facing new challenges every day, it is important for us to stop and highlight these frontline ...
It is common knowledge that supplier quality is a critical piece of any MedTech QMS. No matter which regulatory ...
The new EU Medical Device Regulation is set to enter into force on May 26, 2021, which is less than a month away ...
If you have developed a medical device, you know how important the concept of traceability is. Every facet of the ...
FDA played a key role in the negotiations of the United States-Mexico-Canada Agreement. The agreement entered into ...
Ready to learn more about working with us?
