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Date: 2015-11-27 10:53:15Pharmaceutical 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 AgencyAdd to Reading ListSource URL: www.hma.euDownload Document from Source WebsiteFile Size: 199,68 KBShare Document on Facebook |
Reset Form APPLICATION FOR PLAN REVIEW State FormR2Indiana State Department of Health Food Protection ProgramDocID: 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 cleDocID: 1rj2G - View Document | |
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MARYLAND DEPARTMENT OF THE ENVIRONMENT APPLICATION FOR TEMPORARY ELECTRONIC REPORTING WAIVER FACILITY INFORMATION Facility Name Facility AddressDocID: 1qAcy - View Document | |
TECHNICAL OPERATIONS MANUAL FOR ELECTRONIC FILING IN MONTANA STATE COURTS State of Montana Judicial BranchDocID: 1qlYz - View Document |