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This Week in Quality Digest Live
FDA Compliance Features
Stephanie McArdle
The agency seeks to balance expedient exemptions against public transparency about medical devices
Grant Ramaley
European MDR update: Lowest risk medical devices must comply by May 26, 2020
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

More Features

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

More News

Quality Digest Live -- January 18, 2013

Video Information

Story links for January 18, 2013

 

60 Minutes' Robotic 'March of the Machines' Criticized

Using Prizes to Spur Innovation

European Commission Addresses Notified Body Abuse
An interview with Grant Ramaley, Director of Regulatory Affairs, Aseptico

When Stories Work Better Than Facts

What Gets Measured Also Gets Managed
An interview with Kari Miller, senior director of industry solutions and product management at Pilgrim Software

 

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