Greenlight Guru Blog Introducing Document Comparison: Boost Audit Readiness, Accelerate Training, and Streamline Approvals

There may be hundreds-even thousands-of documents living in the quality management system (QMS) of a medical device company. And many, if not most, of those documents will need to be changed over their lifetime. There are endless reasons to change a document, such as a standard operating procedure (SOP) that needs to be updated to reflect a new method for assembling a device.