Transcription of Harmonised Technical Guidance for Non-eCTD …
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Technical NeeS Guidance Page 1 of 19 Guidance for Industry on Providing Regulatory Information in electronic Format Harmonised Technical Guidance for Non-eCTD electronic Submissions (NeeS) for human medicinal products in the EU Version October 2013 Technical NeeS Guidance Page 2 of 19 Table of Content 1 Introduction .. 32 General considerations .. Scope .. Types of product Types of submission Types of procedures Exceptions Structure of submissions .. Dossier Structure Table of Contents and bookmarks Moving to NeeS format applications .. General Submission Considerations .. File and folder structure Submission numbering File Naming Placement of Documents Correspondence.
Technical NeeS Guidance v4.0 Page 1 of 19. Guidance for Industry on Providing Regulatory Information in Electronic Format . Harmonised Technical Guidance for
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Electronic, Technical Specification, Electronic signatures, Draft Guidance for Industry, Implementing Title 21 CFR Part, Electronic Records ; Electronic Signatures) in, Engineering Specification, November 2011, Specification, PERFORMANCE QUALIFICATION PROTOCOL FOR, EXAMPLE VALIDATION SPREADSHEET SERVING