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This document gives a basic overview of the KNX certification procedure when using the ON Semiconductor KNX Transceiver NCN5120 and a KNX certified system stack, primarily aimed at newcomers to the
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What is AND9102/D?
AND9102/D is a specific form used by the U.S. Food and Drug Administration (FDA) for the submission of drug application data, particularly for over-the-counter (OTC) medications.
Who is required to file AND9102/D?
Manufacturers of over-the-counter (OTC) drug products are required to file AND9102/D when seeking approval for their drug applications.
How to fill out AND9102/D?
To fill out AND9102/D, applicants should follow the guidelines provided in the FDA's instructions, ensuring all required fields are completed and the necessary supporting documents are attached.
What is the purpose of AND9102/D?
The purpose of AND9102/D is to provide the FDA with the necessary information to evaluate the safety and efficacy of over-the-counter drug products before they can be marketed.
What information must be reported on AND9102/D?
AND9102/D must include information such as the product formulation, labeling, manufacturing processes, stability data, and evidence of safety and effectiveness for the intended uses.
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