The medical device market is certainly a burgeoning star but medical device companies could still generate even more revenue and enterprise success
To learn how medical device companies can streamline compliance and quality management processes faster and more effectively, please feel free to download the following MasterControl content:
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MasterControl works hand in hand with medical device companies to provide the compliant ready document control, strict audit-trail tracking and the related quality process technologies that med device companies need to streamline submissions documentation, MDRs, design files, audits and quality related processes such as deviations tracking, nonconformance tracking, customer complaints handling, equipment calibration, CAPA investigations, change control and training.
Medical device companies regulated by the FDA are required to validate their software solutions. MasterControl provides validation services as well a validation related products such as the Transfer OQ and PQ Library solutions.
Additional services include the following:
For more information in regards to the software solutions that can greatly affect the medical device market for the better, please feel free to contact a MasterControl representative.