FDA PMA - Medical Device Premarket Approval
An FDA PMA application is key to obtaining FDA approval and permission to market Class III (and some Class II) medical devices.
Since the FDA medical device premarket approval application is the most demanding FDA submission, medical device companies may find it especially difficult to collect, manage and process the information it comprises for submission and approval.
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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:
- MasterControl MD
- MasterControl Documents
- MasterControl Processes
- MasterControl Nonconformance
- MasterControl Deviations
- MasterControl Customer Complaints Handling
- MasterControl Audit
- MasterControl Equipment Calibration
- MasterControl Equipment Maintenance
- MasterControl CAPA
- MasterControl Projects
- MasterControl Change Control
- MasterControl Training
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.
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