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Welcome to Sangam Global Pharmaceutical & Regulatory Consultancy (SGPRC) established in 2010, we are a group of Highly qualified professional having more than10 yearsof vast experience in Pharmaceutical Regulatory Affairs,providing High quality Pharmaceutical Dossier Service to many Pharmaceutical companies. Our aim is to provide High Quality Pharmaceutical Dossier in all over the world.Pharmaceutical Dossier is an Important & Critical part of Product Registration process, which is need to submit in Food & Drug Administration of the concerned Ministry of Health, of Regulatory Authority.Different Regulatory Authority published their Standard format according to country Guidelines.Common Pharmaceutical Dossier which is widely used in the Pharmaceutical Industry are:CTD DossierACTD DossiereCTD DossierCountry Specific Registration DossierCTD Format DossiersThis Format of Dossier is an Important & widely used Dossier format in most of the country, This format of any registration application for Marketing Authorization Dossier is submitted to Food and Drug Authority or Ministry of health or any other equivalent authority along with other required documents.SGPRC provide registration file for drug product registration in various countries all over the world for many Pharmaceutical Company in INDIA & for our International Business Associates.SGPRC Provides Registration Dossier service in Dossier Compilation, Dossier Preparation & Dossier Review in accordance to the respective Regulatory Authority Guidelines.Pharmaceutical Dossier Compilation, Review and writing as per CTD Format (Common technical Document)Common Technical Document Consists of the following Modules with the number of the required Documents.Module 1 Administrative Information & Prescribing InformationModule 2 - Common Technical Documents SummariesModule 3 QualityModule 4 Non Clinical Study ReportModule 5 Clinical Study ReportCTD Format Dossier is widely used in semi regulated & regulated market like CIS Countries, Middle East countries, European Union, USA, Australia, African Countries, Canada, Japan, etcACTD Format DossiersACTD Format Dossier is also Described as ASEAN CTD Dossier, ASEAN Common Technical Dossier (ACTD) provides a common format for the preparation of well-structured Common Technical Dossier applications for submission in ASEAN regulatory authorities for the registration of pharmaceuticals for human use. ACTD format significantly reduce the time and resources needed to compile applications for registration. Regulatory reviews and communication with the applicant is facilitated by a standard document of common elements.This guideline merely demonstrates an appropriate write-up format for acquired data. However,applicants can modify, if needed, to provide the best possible presentation of the technical information, in order to facilitate the understanding and evaluation of the results upon pharmaceutical registration.Dossier writing and compilation as per ACTD Format.Asian Common Technical Documents consists of following parts.Part I Administrative Data and Product InformationPart II Quality DocumentsPart III Non Clinical DocumentsPart IV Clinical Documents.ACTD Format is Asian harmonization for Common technical Documents used in Asian Countries like Vietnam, Thailand, Singapore, and Malaysia, Philippines & in Member States.eCTD Format DossierThis format of Registration Dossier is an electronic format for CTD Dossier, Submission in eCTD format should be in accordance with the current ICH M2 EWG eCTD specification, Electronic files should be in accordance with the Guidance for Industry on Providing Regulatory Information in Electronic Format. The eCTD is an interface for the pharmaceutical industry to transfer regulatory information with various regulatory agencies. The content is based on the Common Technical Document (CTD) format. It was developed by the International Conference on Harmonisation (ICH) Multidisciplinary Group 2 Expert Working Group (ICH M2 EWG).NeeS format DossierRequirements for the submission of Non-eCTD electronic Submissions (NeeS). A separate EU guidance document covering eCTD submissions, which is regarded as the principal electronic submission format in EU. A NeeS format submission can normally be started with any initial, variation or renewal MA submission.