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WASHINGTON METROPOLITAN AREA TRANSIT COMMISSION WASHINGTON, ORDER NO. IN THE MATTER OF: DC 4801 Served March 28, Application of WASHINGTON SHUTTLE INC., Trading as SUPERSHUTTLE, ) for a Certificate
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What is in-vitro registration certificate for?
The in-vitro registration certificate is used for registering in-vitro diagnostic medical devices.
Who is required to file in-vitro registration certificate for?
Manufacturers, importers, and distributors of in-vitro diagnostic medical devices are required to file the registration certificate.
How to fill out in-vitro registration certificate for?
The in-vitro registration certificate can usually be filled out online through a designated portal or platform specified by the regulatory authority. The exact process may vary depending on the country or region.
What is the purpose of in-vitro registration certificate for?
The purpose of the in-vitro registration certificate is to ensure that in-vitro diagnostic medical devices meet the necessary regulatory requirements for safety and performance before they can be marketed and sold.
What information must be reported on in-vitro registration certificate for?
The exact information required on the in-vitro registration certificate may vary depending on the regulatory authority and country. However, common information includes details about the device, its intended use, technical specifications, manufacturing processes, and any clinical data or studies supporting its performance. Other information may include details about the manufacturer, importer, and distributor.
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