Design Control Process Automation

Software to Automate Design Control Processes Including the Management of Design History Files (DHF) and Other Critical Documents Throughout the Entire Product Development Process

Per 21 CFR Part 820, "Each manufacturer of any class III or class II device shall establish?and maintain the procedures to control the design of the device in order to ensure that specified design requirements are met." Compliance with this regulation is documented in the Design History File (DHF) and results in the creation and management of many documents specific to the development history of the medical device.


Product Information

Discover how MasterControl software can manage your processes, all while mitigating risk, improving speed-to-market, and generating ROI.

Product Data Sheets

Educational Materials

Get insider information about the most relevant issues, and how to navigate and overcome the complexities of FDA regulations.

Interactive and Live Demonstrations
White Papers

Design Control Process Automation for GxP Process

MasterControl automates medical device GxP processes to improve efficiency and speed time to market. Processes include:

  • Design Control
  • Corporate and Supplier Compliance
  • Production / Manufacturing Support
  • Labeling and Promotion