Provision No. 2096/2022

Information

Type

Regulation

Regulated products

IVDMD, Medical Devices

Topics

Registration Of Medical Products

Published

January 1, 2022

Last updated

January 1, 2022

Description

The application for Renewal of the Good Manufacturing Practices Certificate for manufacturers and/or importers of medical products and/or diagnostic products for in vitro use governed by ANMAT Provision No. 7425/13, as amended, shall be processed in accordance with the provisions of this provision. B.O. March 23rd, 2022.

Organization

Country / Region

Argentina

License

Creative Commons Attribution 4.0

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