Preventive Process for Regulatory Compliance

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STEPS TO IMPLEMENT QUALITY MANAGEMENT SYSTEM


1 DOCUMENTS Complete detail about the organization's structure, procedures, and resources to give a quality product or service to the customer.


2 TRAINING It is specially framed for providing the employees with important qualities for medical devices with the requirements of ISO.


3 DEVICE FILE In this record, the content must includes product description, instructions label, specification of component.


4 INTERNAL Checking the safety and effectiveness objectives of the medicative appliances they sell and ensure that adequate to the customer by the person inside the company.


5 CERTIFICATION Auditor will examine all medical devices and give a review and must prove that compliant with the concerned standards.


PRESENTED BY

CONTACT DETAILS

919.313.3960 Morrisville, NC Methodsense.com


THANK YOU


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