Consultants for WHO-PQ, WHO-EUL & QMS (ISO13485) & Regulatory (CDSCO MDR 2017, EU, USFDA, MDSAP). Medical Device & IVD

Intrust started consultancy amidst changing regulation (MDR 2017, EU MDR & IVDR, MDSAP) requiring highest level of compliance to ISO 13485 based QMS from Design to Post Market Surveillance and other regulatory targets. This means improved quality of people, products and processes which can sustain stringent & unannounced audits.  Even notified bodies are re-qualified for this purpose.  

Intrust Consulting

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Intrust Consulting

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