Global Certificate in AM Regulations Compliance Framework
-- ViewingNowThe Global Certificate in AM Regulations Compliance Framework course is a comprehensive program designed to meet the growing industry demand for experts knowledgeable in additive manufacturing (AM) regulations. This course emphasizes the importance of understanding and implementing regulatory compliance in AM, a critical aspect of the industry that ensures safety, reliability, and quality.
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โข Global AM Regulations Overview: Understanding the global landscape of Additive Manufacturing (AM) regulations, including key players and regulatory frameworks. โข AM Regulations in the US: A deep dive into AM regulations in the United States, including FDA and FAA regulations. โข AM Regulations in the EU: An exploration of AM regulations in the European Union, including the Medical Device Regulation and Machinery Directive. โข AM Regulations in Asia: A review of AM regulations in Asia, including Japanese Pharmaceutical and Medical Device Act and Chinese CFDA regulations. โข AM Quality Management Systems: An examination of quality management systems, including ISO 9001 and AS 9100, and their application to AM. โข AM Standards and Guidelines: An overview of AM standards and guidelines, including ASTM, ISO, and SAE standards. โข AM Intellectual Property Protection: Understanding the legal and regulatory considerations for protecting intellectual property in AM. โข AM Risk Management: An exploration of risk management in AM, including risk assessment, mitigation, and monitoring. โข AM Data Management: A review of data management considerations in AM, including data security, privacy, and interoperability.
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