Document Management

This blog is the second of a three-part series on QMS implementation best practices. Read the first blog article for a best practices approach for organizing and managing a QMS implementation [...]

Regulators such as FDA, European Commission (EC), ISO 13485  require a product complaint management system that is effective for resolving product quality issues and improving patient safety. [...]

Have you ever been part of a process that had a failure or two? Perhaps you’ve been on a team that missed a deadline because something didn’t go as expected.  Most of us have. In many cases, the [...]