Docusys Corporation

medical devices

About

Founded in 1994, Docusys Corporation is a trusted partner in quality management systems (QMS) and regulatory affairs for the medical device, aerospace, and manufacturing industries. With over 30 years of expertise and more than 350 clients worldwide, we help organizations—from startups to global corporations—achieve compliance, streamline operations, and accelerate growth. Our team holds Lead Auditor certifications in ISO 9001, ISO 13485, MDSAP, and AS9100/AS9120, bringing deep knowledge of international standards and regulatory requirements. We provide end-to-end support including documentation, implementation, internal audits, regulatory submissions, training, and outsourced quality management. Whether you are a startup preparing your first submission or an established company expanding globally, Docusys delivers practical, effective, and tailored solutions that minimize bureaucracy while meeting and exceeding industry expectations.

Technologies

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Keywords

iso 9001 medical device mdsap aerospace quality management systems regulatory affairs & aerospace quality management systems iso 13485 regulatory affairs as9100 as9120 risk management quality management systems medical equipment manufacturing regulatory strategy aerospace standards regulatory submissions aerospace audits other scientific and technical consulting services ce marking japan jpal aerospace lead auditor health canada submissions medical device regulations aerospace quality systems quality system training medical device license submissions medical device regulatory strategy mdsap certification eu mdr compliance b2b regulatory consulting

Location

Montreal, Quebec, Canada, H2L

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