Document control is an important process in any company’s quality system. The FDA requires that certain industries properly and clearly document their SOPs and other activities. This can lead to a huge document escalation if you aren’t careful. Quality management software, however, has given companies a new option.
If you integrate a software solution like this, you will have a central repository for all documentation, and you will be able to automate the assignment or routing of document scheduling, follow-up, tracking, and review. Also, everyone will have access to the necessary documents, and management will quickly be able to see what has received approval and what is still in the system.
