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Non-Material Amendment Weekly list from 19/04/2021 to 23/04/2021This list of applications for nonmaterial amendments are for information purposes only. There are no consultations on this type of application.

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What is scrutiny of covid-19 instruments?

Scrutiny of covid-19 instruments is a process of reviewing and examining the documents related to covid-19 testing kits, vaccines, or other medical equipment.

Who is required to file scrutiny of covid-19 instruments?

Manufacturers, distributors, or importers of covid-19 instruments are required to file scrutiny of covid-19 instruments.

How to fill out scrutiny of covid-19 instruments?

To fill out scrutiny of covid-19 instruments, the required information must be accurately documented in the specified form provided by the regulatory authority.

What is the purpose of scrutiny of covid-19 instruments?

The purpose of scrutiny of covid-19 instruments is to ensure the quality, safety, and efficacy of the covid-19 related products being used in the market.

What information must be reported on scrutiny of covid-19 instruments?

Manufacturing details, clinical trial data, safety reports, and any adverse events related to the covid-19 instruments must be reported on scrutiny of covid-19 instruments.

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