##  [Aligning Supplier Evaluation Practices with 21 CFR 820 and ISO 13485 Requirements](/index%2Ephp/white-papers/aligning-supplier-evaluation-practices-with-21-cfr-820-and-iso-13485-requirements) 

- [Medical Devices](/index%2Ephp/white-papers-categories/medical-devices)
- [Quality, Compliance, & Audit (QMS)](/index%2Ephp/white-papers-categories/quality-compliance-audit-qms)





 ![Aligning Supplier Evaluation Practices with 21 CFR 820 and ISO 13485 Requirements]()

Supplier assessment is significant for ensuring product quality, Compliance with regulations, and business excellence in the medical device sector. Organizations must make their supplier assessment practice compatible with ISO 13485:2016 and 21 CFR 820 requirements.

This whitepaper delves into the intricacies of supplier assessment from three (3) essential viewpoints: **Supplier Selection** and **Appraisal**, **Risk-Based Approach**, and **Performance Monitoring**. By knowing and executing these strategies, medical device companies can improve supply chain dependability, mitigate risks, and adhere to Regulatory requirements.



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