|
|
|
Information:
|
ICH is a joint initiative involving both regulators and research-based industry representatives of the European Union, Japan and the USA in scientific and technical discussions of the testing procedures required to assess and ensure the safety, quality and efficacy of medicines.
This OID is used by the M2 Expert Working Group for identification of relevant artifacts. M2 is responsible for the development and maintenance of Electronic Standards for the Transfer of Regulatory Information (ESTRI) for ICH and in collaboration with external standards development organizations such as Health Level 7 (HL7), ISO and CEN.
|
|
First Registration Authority
|
|
|
|
|
Creation date:
|
30 June 2011
|
|
Disclaimer: The owner of this site does not warrant or assume any liability or responsibility for the accuracy, completeness, or usefulness of any information available on this page (for more information, please read the complete disclaimer).
All rights reserved, Orange © 2024 |