FDA Considering Whether an FDA-Regulated Product Involves the Application of Nanotechnology

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Considering Whether an FDA-Regulated Product Involves the Application of Nanotechnology[附网盘链接]由Food And Drug Administration于不久之前发布,适用于United States。

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Considering Whether an FDA-Regulated Product Involves the Application of Nanotechnology[附网盘链接]
Considering Whether an FDA-Regulated Product Involves the Application of Nanotechnology[附网盘链接](截图)

 

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TABLE OF CONTENTS I. INTRODUCTION AND SCOPE II. DISCUSSION A. Points to Consider B. Rationale for Elements within the Points to Consider 1. Material or end product that is engineered to have certain dimensions or exhibit certain properties (in Points 1 and 2) 2. Material or end product (in Points 1 and 2) 3. At least one external dimension, or an internal or surface structure, in the nanoscale range (approximately 1 nm to 100 nm) (in Point 1) 4. Properties or phenomena attributable to dimension(s) (in Point 2) 5. Dimension(s) of up to one micrometer (1,000 nm) (in Point 2) III. CONCLUSION IV. REFERENCES 2

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