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MEDICAL DEVICES REGULATIONS 2002: REGULATIONS 19 and 30 FORM RG2 REGISTRATION OF PERSONS RESPONSIBLE FOR PLACING DEVICES ON THE MARKET PART 1: About the notification Please read the accompanying guidance
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What is mhra registration form rg2?
The MHRA registration form RG2 is a form that needs to be filled out by companies or individuals who are involved in the manufacturing or distribution of medical devices. It is a registration form that is required by the Medicines and Healthcare products Regulatory Agency (MHRA) in the United Kingdom.
Who is required to file mhra registration form rg2?
Companies or individuals who are involved in the manufacturing or distribution of medical devices in the United Kingdom are required to file the MHRA registration form RG2.
How to fill out mhra registration form rg2?
To fill out the MHRA registration form RG2, you will need to provide information about your company or yourself, including contact details, the types of medical devices you manufacture or distribute, and proof of compliance with relevant regulations and standards. The form can be filled out online or in paper format and must be submitted to the MHRA.
What is the purpose of mhra registration form rg2?
The purpose of the MHRA registration form RG2 is to ensure that companies or individuals involved in the manufacturing or distribution of medical devices in the United Kingdom are compliant with relevant regulations and standards. It allows the MHRA to have a record of all medical device manufacturers and distributors operating in the country.
What information must be reported on mhra registration form rg2?
The MHRA registration form RG2 requires the reporting of information such as company contact details, types of medical devices manufactured or distributed, and proof of compliance with relevant regulations and standards. Additional information may be required depending on the specific circumstances of the company or individual.
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