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Med QMS

Medical Devices QMS and Regulatory Affairs Melbourne

For all your Medical Device Quality Assurance and Regulatory Affairs needs

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Article

Article
quality system and regulatory affairs

November 1, 2019

Corrective and Preventive Action (CAPA) – The three most common mistakes

Are you familiar with the CAPA process? Having a Corrective and Preventive Action (CAPA) process is a mandatory requirement of most Quality Management Systems standards. If used correctly,

Category iconArticle,  CAPA

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Med QMS

For all your Quality Assurance and Regulatory Affairs requirements.

+61 410 717 106

alexander@medicalqms.com.au

Melbourne based

Elsternwick VIC 3185
Australia

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With 20 years’ experience in the medical device industry, both managing Quality, and Regulatory Affairs and as an active auditor, we can be counted on to deliver the systems, documentation and advice required.
We pride ourselves on having achieved 100% compliance for all our clients. Continue reading …

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