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This Week in Quality Digest Live
FDA Compliance Features
Jon Speer
Lessons from the medical device industry
Matthew M. Lowe
Three-quarters of life sciences CIOs and IT execs say security risks are main reason for opposing cloud technologies
AssurX
Questions linger about FDA processes that seem to favor medical device companies
Matthew M. Lowe
Confronting the fear of being displaced by machines

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FDA Compliance News
Creates adaptive system for managing product development and post-market quality for devices with software elements
VQIP allows for expedited review and importation for approved applicants that demonstrate safe supply chains
An invite from Alcon Laboratories
Intended to harmonize domestic and international requirements
The FDA wants medical device manufactures to succeed, new technologies in supply chain managment
Pharma quality teams will have performance-oriented objectives as well as regulatory compliance goals
Strategic investment positions EtQ to accelerate innovation efforts and growth strategy
The FDA’s RMAT designation goes live

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Quality Digest Live -- January 25, 2013

 
 

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