In the News...
U.S. Can Improve Medical Device Approval
Process While Ensuring Safety
The United States does not have to choose between the vitality of its medical device industry or the health of its people, U.S. Sen. Al Franken said in an interview at the Design of Medical Devices Conference hosted by the University of Minnesota. It is possible to improve both.
The United States does not have to choose between the vitality of its medical device industry or the health of its people, U.S. Sen. Al Franken said in an interview at the Design of Medical Devices Conference hosted by the University of Minnesota. It is possible to improve both.
Related Event:
Regulatory Information Management Conference
April 24-25 | Philadelphia
April 24-25 | Philadelphia
The Regulatory
Information Management (RIM) Conference features business and
technology tracks. The business track will focus on ways to obtain and manage
regulatory information and the related organizational impact. The technology
track will explore ways to create a business case for an RIM system, submission
standards of regulatory information, manage the information, and identify key
business drivers for establishing a global RIM system.
Register Now
No comments:
Post a Comment