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Hostrin Life Sciences service offering dossier as NON-ACTD, CTD & eCTD Dossier services  as per country specific guideline and service full report of technical writing services. This service meets the clients need, that are closely matched to industry documentation conventions.Generation of all documentation Stability reports compiled in accordance with CGMP-ICH preferred format which leads to ready incorporation include dossier submissions Compilation stability testing...

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Administrative Document is a set of specifications for application dossier, for the registration of Medicines and designed to be used across Europe, Japan and the United States. It is an internationally agreed format for the preparation of applications regarding new drugs intended to be submitted to regional regulatory authorities in participating countries. It was developed by the European Medicines Agency (EMA, Europe), the Food and Drug Administration (FDA, US)...

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CTD Format Dossier is widely used in semi regulated & regulated market like CIS Countries, Middle Eastern countries, European Union, USA , Australia , Canada and Japan etc.,Dossier writing and compilation as per ACTD Format – Asian Common Technical DocumentPart I – Administrative Documents Part II – Quality Documents Part III – Non Clinical Documents Part IV – Clinical Documents.ACTD Format is Asian...

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