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U.S. NUCLEAR regulatory COMMISSION NRC For RR. TC 1?1,provoke by CUA0REGISTRATION CERTIFICATE IN VITO TESTING WITH BYPRODUCT MATERIAL UNDER GENERAL LICENSEIo0 CF3m.piouo0Section 31.11 of 10 CFR 31

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Step 8: Once you receive the registration certificate, keep it in a safe place and ensure its validity period is adhered to.

Who needs registration certificate for in-vitro?

01

Medical laboratories or institutions conducting in-vitro diagnostic testing.

02

Manufacturers or importers of in-vitro diagnostic medical devices.

03

Any entity involved in the distribution or sale of in-vitro diagnostic medical devices.

04

Researchers or scientists performing in-vitro experiments or studies.

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What is registration certificate for in-vitro?

The registration certificate for in-vitro is a document required for approval and registration of in-vitro diagnostic medical devices.

Who is required to file registration certificate for in-vitro?

Manufacturers or distributors of in-vitro diagnostic medical devices are required to file the registration certificate.

How to fill out registration certificate for in-vitro?

The registration certificate for in-vitro can be filled out by providing the necessary information about the device, its intended use, and the manufacturing details.

What is the purpose of registration certificate for in-vitro?

The purpose of the registration certificate for in-vitro is to ensure that the medical devices meet the required standards and are safe for use.

What information must be reported on registration certificate for in-vitro?

The registration certificate must include details about the device, its intended use, manufacturing process, quality control, and any relevant certifications.

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