Provision No. 2580/2022

Name: Provision No. 2580/2022
Creator: National Administration of Drugs, Food and Medical Devices
License: https://creativecommons.org/licenses/by/4.0/
Keywords: amendments,applications,certificates,diagnostics,gmp,good-manufacturing-practice,importers,manufacturers,manufacturing,practices,provisions,regulations,renewal

Information

Original link

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 and its amendments shall be processed in accordance with the provisions of this provision. B.O. April 6, 2022.

Organization

National Administration of Drugs, Food and Medical Devices (ANMAT) 🇦🇷

Country / Region

Argentina

License

Creative Commons Attribution 4.0

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Disposición N° 2580/2022

Updated on January 1, 2022

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URL: https://www.boletinoficial.gob.ar/detalleAviso/primera/260510/20220406
Permalink: https://data.openrid.co/en/datasets/r/68e838fd-6d39-46f7-ac59-8ee9aa1f5366
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Created on: January 1, 2022
Modified on: January 1, 2022