<--- Back to Details
First PageDocument Content
Pharmaceutical industry / Pharmaceuticals policy / Drug Master File / QP / Qualified person
Date: 2015-11-27 10:53:15
Pharmaceutical industry
Pharmaceuticals policy
Drug Master File
QP
Qualified person

Q&A on QP declaration Meeting with IPs on DCP_MRP Improvements 16. November 2016 Inger Heggebø The Norwegian Medicines Agency

Add to Reading List

Source URL: www.hma.eu

Download Document from Source Website

File Size: 199,68 KB

Share Document on Facebook

Similar Documents

Reset Form  APPLICATION FOR PLAN REVIEW State FormR2Indiana State Department of Health Food Protection Program

Reset Form APPLICATION FOR PLAN REVIEW State FormR2Indiana State Department of Health Food Protection Program

DocID: 1rpiu - View Document

Release Notes for Harmonised Technical Guidance for eCTD Submissions in the EU v3.0 This document highlights the changes incorporated in version 3.0, in comparison with version 2.0, of the eCTD guidance document. For cle

Release Notes for Harmonised Technical Guidance for eCTD Submissions in the EU v3.0 This document highlights the changes incorporated in version 3.0, in comparison with version 2.0, of the eCTD guidance document. For cle

DocID: 1rj2G - View Document

EU Module 1 Specification - Annex VersionRelease Notes November 2011

EU Module 1 Specification - Annex VersionRelease Notes November 2011

DocID: 1qRm8 - View Document

MARYLAND DEPARTMENT OF THE ENVIRONMENT APPLICATION FOR TEMPORARY ELECTRONIC REPORTING WAIVER FACILITY INFORMATION Facility Name Facility Address

MARYLAND DEPARTMENT OF THE ENVIRONMENT APPLICATION FOR TEMPORARY ELECTRONIC REPORTING WAIVER FACILITY INFORMATION Facility Name Facility Address

DocID: 1qAcy - View Document

TECHNICAL OPERATIONS MANUAL FOR ELECTRONIC FILING IN MONTANA STATE COURTS State of Montana Judicial Branch

TECHNICAL OPERATIONS MANUAL FOR ELECTRONIC FILING IN MONTANA STATE COURTS State of Montana Judicial Branch

DocID: 1qlYz - View Document