Quality Management
Developing a QMS?
Know which standards apply?
Need auditing?
The strategic implementation of the right Quality Management System (QMS) at the right time for your medtech venture is what Psephos offers, from concept to commercialisation and beyond.
Services to Support Your Product Development:
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Identification of appropriate QMS standards (e.g. ISO 13485) and regulations (e.g. EU MDR) that apply to your company and device
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Tiered approach to writing, implementing and operating your QMS
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UKCA Integrated Document Control and Related QMS Activities ServiceMarking
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Auditing and Corrective Action Planning and Implementation
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Training and development of your team to gain the most from the use of your compliant QMS
Welcome to our 4-part video series which provides an overview of the importance of a Quality Management System (QMS) in the medical device industry.
