Provision No. 7425/13

Name: Provision No. 7425/13
Creator: National Administration of Drugs, Food and Medical Devices
License: https://creativecommons.org/licenses/by/4.0/
Keywords: authorization,diagnostics,provisions,regulations

Information

Original link

Type

Regulation

Regulated products

IVDMD, Medical Devices

Topics

Qualification Of Medical Product Manufacturing And/Or Importing Companies

Published

January 1, 2013

Last updated

January 1, 2013

Description

The activities of manufacture and importation of medical products and diagnostic products for "in vitro" use may only be carried out after prior authorization of the company's operation according to ANMAT Provision No. 2319/02 (T.O. 2004) and under the control of this National Administration.

Organization

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

Country / Region

Argentina

License

Creative Commons Attribution 4.0

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1 Main file

Disposición Nº 7425/13

Updated on January 1, 2013

pdf

URL: https://www.anmat.gob.ar/boletin_anmat/BO/Disposicion_7425-2013.pdf
Permalink: https://data.openrid.co/en/datasets/r/1be5e718-a119-4bef-a4e1-13ae024fb3e8
MIME Type: application/pdf

Created on: January 1, 2013
Modified on: January 1, 2013