How does FDA Medical Device Premarket Approval work?
MasterControl provides a variety of software solutions that are designed to streamline compliance (FDA, ISO, CLIA, etc.), quality-related processes, training and document management and control. These solutions can be combined, implemented and launched within one integrated platform that can be accessed via the Internet from virtually anywhere in the world. MasterControl provides functionality that is essential for compliance concepts such as deviations management, document management, tracking (audit trails), document location, logistics information, etc. With MasterControl, management of an FDA PMA application and other compliance related documents becomes a far simpler process.
MasterControl FDA PMA (Premarket Approval) Solutions
MasterControl provides the following solutions:
- Documents MasterControl
- MasterControl Processes
- MasterControl Non conformité
- MasterControl Deviations
- MasterControl Customer Complaints Handling
- MasterControl Audit
- MasterControl Equipment Calibration
- MasterControl Equipment Maintenance
- MasterControl CAPA
- MasterControl Projects
- MasterControl Change Control
- Formations MasterControl
For More Information on FDA Medical Device Premarket Approval
Contact a MasterControl representative to learn more about the web-based, electronic software solutions that help streamline the tasks and processes associated with FDA medical device premarket approval submissions.