Additional Content
Complaint Handling as an Integral Part of FDA and ISO Compliance
Effective complaint handling is not just a good business practice, but a critical compliance requirement in FDA and ISO environments.
Guidelines For The European Medical Device Vigilance System
"How-to" information for medical device companies complying with regulations standardized by the MDDs (Medical Device Directives). Access the MEDDEV-5 when developing quality and compliance processes.
MasterControl eMDR™
The FDA requires medical device manufacturers to report any adverse events to the agency.
MasterControl Customer Complaints™
Address the key complaints-handling challenges of different sources, disconnected processes and an inefficient complaint process by automating and integrating your complaint handling.
Px Solution Overview
The MasterControl Postmarket Excellence™ solution streamlines the capture and documentation of postmarket feedback from customer complaints and surveys to manage risk and ensure compliance.
MasterControl Postmarket Excellence™ Solution Overview
The MasterControl Postmarket Excellence™ solution is the next generation of integrated surveillance, customer feedback and quality management processes.
4:06Fagron Uses MasterControl's Cloud Quality Management for their Personalized Medicine
Fagron is an international personalized medicine pharmaceutical company that recently started using MasterControl to improve its quality and manufacturing processes.
27:30Best Practices in Post Market Intelligence
Medical device companies are required to conduct post-market surveillance (PMS) on their devices to maintain high product quality and safety.