Feb 3, 2023
FDA
The new article describes the recommended content and highlights the key points to be considered in this respect. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare products, has published a...
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Feb 3, 2023
FDA
The new article addresses the aspects related to the scope of events eligible for the program, as well as to its general conditions. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare...
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Feb 2, 2023
FDA
The new article describes the recommended content and highlights the key points to be considered in this respect. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare products, has published a...
Read More
Feb 2, 2023
FDA
The new article provides an overview of the regulatory requirements related to the information on human factors to be submitted when applying for marketing approval. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in...
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Jan 27, 2023
FDA
The new article addresses the aspects related to supplemental reports medical device manufacturers should submit and also provides an overview of the summary reporting instructions. Table of Contents The Food and Drug Administration (FDA or the Agency), the US...
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