13 item(s)
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Read this article and find out more about 3 pillars for effective supplier management and how they help to build a system that is accurate, responsive, and efficient.
3 Pillars of Effective Supplier Management
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Read this article to see a step-by-step guide to holding an effective workplace safety conversation.
EHSM: A 5-Step Guide for a Safety Conversation
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How to choose the right suppliers, service providers and sub-tier suppliers, and how to monitor them to ensure FDA compliance.
Managing your Medical Device suppliers – Tips for ensuring they are truly FDA compliant
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Read this article and find out more on how a Document Control System may help companies to ensure regulatory compliance.
Why my electronic “Document Control System” may only be a “Document Management System”
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Device Master Records and Medical Device files are FDA requirements. How do they compare?
Device Master Records and Medical Device Files – How Do They Compare?
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The EHS department can be housed in a wide variety of locations within an organization. What is its optimal placement?
The “Right Home” for Environment, Health and Safety
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The several factors that must be considered when determining the appropriate sample size for process validation.
Process Validation: How many sample sizes do I need?
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The importance of the "risk based approach" for the correct performance and adequate safety of medical devices.
How will ISO 13485:2016 impact your relationship with suppliers?
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The key clauses of ISO 13485 and the business benefits of quality management in the medical devices industry.
ISO 13485 – Medical devices quality management systems
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The key clauses of ISO 14001:2015 and the business benefits of environmental management.
ISO 14001:2015 – Environmental management systems
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The essential modifications in the ISO 14001:2015, in comparison with the last revision dating back to 2009.
ISO 14001:2015. What is new?
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Practical indices or metrics for environmental sustainability.