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.
Tags
Organization
Country / Region
Argentina
License
Creative Commons Attribution 4.0