Provision No. 4930/13

Name: Provision No. 4930/13
Creator: National Administration of Drugs, Food and Medical Devices
License: https://creativecommons.org/licenses/by/4.0/
Keywords: gmp,good-manufacturing-practice,manufacturing,practices,provisions,regulations

Information

Original link

Type

Regulation

Regulated products

Medical Devices

Topics

Qualification Of Medical Product Manufacturing And/Or Importing Companies

Published

January 1, 2017

Last updated

January 1, 2017

Description

Articles 10, 11, 12 and 13 of ANMAT Provision No. 7425/13 are replaced and Articles 10 bis and 12 bis are incorporated in the same regulation (Good Manufacturing Practices for Medical Products). B.O. May 17, 2017.

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 4930/13

Updated on January 1, 2017

pdf

URL: https://www.anmat.gob.ar/boletin_anmat/BO/Disposicion_4930-2017.pdf
Permalink: https://data.openrid.co/en/datasets/r/1e450a7e-c081-40b9-bf18-a660fc2b219a
MIME Type: application/pdf

Created on: January 1, 2017
Modified on: January 1, 2017