Ozette’s Quality Management System (QMS) ensures consistency, reliability, and excellence in operations across all facets of the organization. It is a structured framework that integrates quality principles into all of Ozette’s business processes. Our robust QMS is maintained by a dedicated Quality team with decades of industry expertise. It facilitates compliance with regulatory requirements and fosters continuous improvement, empowering teams to identify and address inefficiencies, mitigate risks, and enhance overall performance.
By establishing clear standards, protocols, and metrics for quality assurance, our QMS not only enhances product and service quality but also cultivates a culture of accountability and excellence.
Ozette is dedicated to ensuring our products meet or exceed applicable guidelines, standards, and regulations.
Current applicable guidelines, standards, and regulations implemented into Ozette’s QMS include:
FDA: The data provided by Ozette is for research/investigational use only, not for use in diagnostic procedures; the performance characteristics of this product have not been established for diagnostic procedures.
EU: Ozette’s platform is a medical device to be used exclusively for clinical investigations.
Ozette is dedicated to ensuring our products meet or exceed applicable guidelines, standards, and regulations.
Current applicable guidelines, standards, and regulations implemented into Ozette’s QMS include:
Ozette complies with all legal requirements for handling personally identifiable data including US HIPAA and EU GDPR. Continuous monitoring enables our organization to meet regulatory requirements and maintain the highest standards of data protection.
Data Protection Officer (DPO): Contact dpo@ozette.com for all EU/UK patient/participant Right to Erasure, Right to Restrict Processing, Right to Data Portability, Right to Object requests.