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Increase your understanding of the essential U.S. medical device regulations, including device classification, organizing pre-market notification ...
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This course presents a detailed overview of the regulatory requirements for the development and manufacture of pharmaceutical products. Individua...
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Gain an understanding of the accepted good principles and practices applicable to the development and implementation of drugs and medical devices ...
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935. Clinical Data Management [Courses]
Learn about the handling, processing, storage, retrieval, and electronic submissions of clinical data. Gain an understanding of the issues and im...
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936. How to Complete Your Program [Student Resources]
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937. How to Complete Your Program [Student Resources]
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This course presents an introduction to the field of regulatory affairs and to the laws and regulations governing healthcare products, including d...
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Learn how to continuously evaluate and perform periodic reporting on the safety, effectiveness, and reliability of a medical device for its intend...
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From concept through development to approval, the Medical Product Life Cycle integrates design, development, validation, and commercialization. Fu...
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