NeeS submission, NeeS publishing, Non-eCTD, NeeS format

Non-eCTD electronic Submission (NeeS) format has been made mandatory in the European Union(EU) from 2003 onwards. When compared to the electronic common technical document (eCTD), NeeS is different in terms of navigating structures. It does not use the XML backbone. It also differs from eCTD with two relevant XML files, the index.xml and eu-regional.xml for the backbone of Modules 2 to 5 and Module 1 for the EU, respectively. As per country specific guidelines, using bookmarks and hyperlinks, the NeeS is based on granular PDF files, electronic tables of contents and electronic navigation.

With a clear-cut understanding and expertise in handling region-specific NeeS requirements, Freyr helps manufacturers navigate through Regulatory dossier compilation for publishing and submissions.

Freyr specializes in creating NeeS submissions for:

Europe - Module 1 Specification, EU NeeS Validation Criteria Australia/New Zealand - NeeS Validation Criteria Gulf Corporation Council (GCC), Saudi Food and Drug Authority (SFDA) NeeS - Module 1 Specification and eCTD Validation Criteria Agency for Medicinal Products and Medical Devices of Bosnia and Herzegovina – (ALMBiH) NeeS for all types of Regulatory submissions Canada NeeS submissions for Clinical Trial Applications (CTAs)