New international Meddev rules challenge complacent organizations
One size does not fit all
The agency’s 2017 goals featured at regulatory professionals conference
A key link in the safety chain
Embrace the total product life cycle
Creating global alliances to meet the challenge
Building out a national system for evidence generation
The curious logic behind prescription drug names
Understand the importance of three overlooked parts: 820, 803, and 806
Laying the foundation for a national system for clinical evidence generation
Robots lighten the laboratory load
A laboratory quality management system is key
FDA offers guidance for working with its Emerging Technology Team
Will this be good for Canada?
Our progress addressing food safety, tobacco use, and antimicrobial resistance
A review of FDA’s effect on medical product safety and oversight
A summary of medical product innovation
FDA defines some terms
A Case for Quality is changing medical device manufacturers focus and FDA’s approach
An industry study recommends five changes for intercenter consultations