ISO 10993
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What is ISO 10993?
ISO 10993 is a set of standards for the biological evaluation of medical devices. It outlines procedures for testing medical devices to assess their potential for adverse biological effects, such as cytotoxicity, sensitization, irritation, and systemic toxicity. The goal of ISO 10993 is to ensure that medical devices are safe for use in humans by minimizing the risk of harm from their materials and construction.
What other technologies are related to ISO 10993?
ISO 10993 Complementary Technologies
ISO 14971
ISO 14971 is a risk management standard for medical devices. It is complementary to ISO 10993, which focuses on biological evaluation, as risk management (ISO 14971) utilizes biological safety data (ISO 10993) as input, and biological safety evaluation considers the risk management process.
ISO 13485
ISO 13485 specifies requirements for a quality management system specific to the medical device industry. While not directly related to biological evaluation like ISO 10993, it provides a framework for managing the design, development, production, and post-market surveillance of medical devices, which indirectly supports the effective implementation of ISO 10993 requirements.
Number of organizations that mention technology
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Which job functions commonly mention ISO 10993?
Toxicologist
1.3% of all Toxicologist jobs mention ISO 10993
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jobs on Sumble
Public Policy
43 Public Policy jobs mention ISO 10993
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jobs on Sumble
Safety Engineer
8 Safety Engineer jobs mention ISO 10993
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jobs on Sumble
Scientist
48 Scientist jobs mention ISO 10993
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jobs on Sumble
Quality Engineer
19 Quality Engineer jobs mention ISO 10993
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jobs on Sumble
Which organizations are mentioning ISO 10993?
Boston Scientific
Health Care and Social Assistance
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