BioWorld MedTech

March 31, 2011

View Archived Issues

Panel gives insight on FDA in development process

ATLANTA – What happens when you put a former FDA reviewer, a CEO who's product failed to garner approval in the U.S., and a researcher, who helps companies navigate the regulatory space in the same room? (Medical Device Daily) Read More

Concerns raised about trends in the teleradiology industry

Read More

International report: EDAP to sell MMS urodynamic diagnostic products in Japan

Read More

Washington roundup: Industry sees double-dipping in IRS device tax regulation

Read More

Deals roundup: Align to 'streamline' procedure with $190M Cadent purchase

Read More

MDD's food for med-tech thought

Read More

People in the News

Read More

Med-Tech Notes

Read More