Customer Complaint Handling Process for Medical Device
Do you know the importance of complaints? Its legal implications? Impact on Post-Market Surveillance? Complaint Handling plays an important role in the device industry and is a regulatory requirement as well as a risk-reduction imperative. Thus, it is extremely important to manage and resolve complaints per regulatory bodies' guidelines and standards.
Medical device
companies must establish a customer complaint-handling process to collect
feedback on potential adverse events that must be reported to the FDA.
IZiel Approach for
Detailed Complaint Handling
·
IZiel
would adopt & implement these steps to help you with compliant handling.
·
Establish
Complaints Handling System
·
Initial
Review and Evaluation
·
Investigation
of Failures
·
Medical
Device Reporting
·
Records
IZiel helps companies
to develop the mechanism of post-market activities. IZiel assists companies to
document the complaints
handling process and helps you to understand the objectives of complaint
handling within the context of the overall Quality System and Corrective and
Preventive Action (CAPA) subsystem.
IZiel works with
medical device companies to effectively manage Complaints Handling, thereby, helping
you provide better, safer, more effective & quality products.
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