The key to an effective postmarket surveillance program is to ensure that the requirements and risks identified early in the development process are continually updated throughout the product lifecycle.

Maintaining “living” design documentation allows companies to better identify, analyze, and respond to potential safety issues. Jama Connect for Medical Devices streamlines and simplifies the PMS process by providing a single source of truth during development and post launch.

Read this datasheet to learn more about key benefits:

• Improve postmarket surveillance by using the same platform during development and post launch
• Reduce risk by managing risk through structured collaboration
• Modernize change management by maintaining a living design documentation file