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Nicol Smith
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Nicol Smith
From Conception to Compliance: A Manufacturer's Guide to the CE Mark Process
CE mark holds outstanding importance for medical device producers aiming to reach the European Market. It acts as a certification that a medical device satisfies
January 23, 2024
Nicol Smith
What are the Responsibilities and Qualifications of ISO 14001 Auditor?
Become an ISO 14001 Auditor to Drive Environmental Excellence. As organizations recognize the value of environmental responsibility, developing and sustaining effective environmental management systems (EMS)
January 19, 2024
Nicol Smith
ISO 13485: Audit Criteria and Certification Process
ISO 13485 is a globally recognised standard that defines the standards for a quality management system (QMS) in the medical device industry. It specialises in
January 17, 2024
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