Additional Content
How to Address the Top 6 Pains in DHF Management
Noncompliance among medical device developers typically falls under two areas: design control and document management. These two critical elements intersect in one place: the design history file.
Managing Change Control to Comply with FDA and EU Regulations
Uncontrolled changes to a pharmaceutical or medical device product have the potential to affect public health and safety.
Reducing the Documentation Burden in FDA Design Control
This white paper shows how medical device developers can better manage all the documentation required for a product launch.
Automating Electronic Engineering Change
Whether expected or unexpected, minor or complex, change is a constant in any manufacturing environment.
Change Control - Continuous Quality Improvement in FDA and ISO Environments
In highly regulated environments, changes to equipment, materials, facilities, design, processes, packaging/labeling, computer systems, documentation, etc. pose a potential risk.
MasterControl Change Control™
MasterControl Change Control™ automates every step of the change control process and keeps your quality system in a state of constant audit- and inspection-readiness.
MasterControl Development Excellence™ Solution Overview
MasterControl has been providing software solutions to highly regulated industries for over 25 years.