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Medical Devices

Medical devices are instruments, equipment, implants, or software used in the diagnosis, treatment, or prevention of medical conditions

he regulatory requirements for the medical devices industry have become more complex in recent years, primarily aimed at ensuring patient safety and protecting the end consumer.

Meet Regulatory Requirements While Protecting Consumers Safety

Meeting regulatory requirements and protecting consumer safety are critical objectives for the medical devices industry

Related Services

In addition to the services mentioned earlier, there are several related services that can further support improving business excellence maturity and sustainable business practices. These services include:

Audit & Certification
Ethical Sourcing
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Steps to Certification
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StandardsMark™ Download
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Audit & Certification
Customized & Second Party Audits
Customized & Second Party Audits Customized audits and second-party audits are two types of auditing approaches that organizations can utilize to meet specific requirements and…
Standards & Schemes
Responsible Recycling© (R2)
R2v3 – The Sustainable Electronics Reuse & Recycling (R2) Standard V3 The practice of refurbishing, de-manufacturing, recycling, and reusing electronics can pose various health and…

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