Regulating manufacturing processes in the medical device industry is challenging. But process signature verification can help manufacturers get a handle on problems before they get out of control.

Regulatory officials and industry scientists participated in a CMC Strategy Forum sponsored by CASSS in July 2015. To ensure that biotech manufacturing processes can consistently deliver high quality ...

A year’s worth of FDA warning letters suggest that API and finished drug manufacturers should strengthen their approach to continued process verification. A year’s worth of FDA warning letters suggest ...

The U.S. Department of Agriculture’s Process Verification Program could provide an avenue for firms to certify the veracity of non-GMO claims without indirectly suggesting that genetic engineering is ...

The integration of advanced microprocessors and sophisticated software has transformed these instruments. Modern magmeters ...

Each year, the Central Processing System (CPS) will randomly select a portion of all aid applications for the verification process. The selection process is controlled by the Federal Government and is ...

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. DENVER (KDVR) — Tuesday marks one week until ...

The Centers for Medicare and Medicaid Services has released a slide deck describing in greater detail the process that they intend to use for pre-enrollment verification of special enrollment period ...