One of the most nebulous aspects of compliance for a medical device manufacturer is knowing whether a process should be verified or validated to ensure its conformity to regulatory requirements.

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.

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 ...

Abstract: In this paper we deal with business process verification for reachability, liveness and deadlock-freeness properties. Actual business process verification techniques use formal methods such ...

Getting a passport in India requires a police verification process, which is a crucial step to ensure the applicant's ...

Managing data at the different stages of the lifecycle, linking disparate systems together, and making the right data available to those who need it is problematic and time consuming. The ...

Microblogging site Twitter has reopened its verification application program for the public after a three-year hiatus to let people make submissions for their profiles to sport the coveted “blue tick” ...