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COMPETENT AUTHORITY (UK)IN VITRO DIAGNOSTIC MEDICAL DEVICES THE MEDICAL DEVICES REGULATIONS 2002: REGULATION 44 FORM RG3 PART 1: Identification of the registration Is the relevant fee enclosed?6200Date
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Registration form rg3 is a form used to register a specific entity or individual with a regulatory authority.
Entities or individuals who meet certain criteria set by the regulatory authority are required to file registration form rg3.
Registration form rg3 can be filled out by providing all the requested information accurately and submitting it to the regulatory authority.
The purpose of registration form rg3 is to ensure that entities or individuals comply with regulations and are registered with the appropriate authority.
Information such as entity or individual details, contact information, and relevant documentation must be reported on registration form rg3.
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