Regulatory Services

CTD’s (Product Dossier) is an necessarily Portion of any enrollment application for Marketing Authorization. Dossier in CTD Format/ ACTD Format or local country format is submitted to Food & Drug Authority or Ministry of health or any other equivalent authority along with other required technical documents and legal manufacturing permissions.

Idealize Pharmaceutical Specialists can assist you entire technical document for Product Registration in different nations all over the world We can Support you to compile and write entire technical document or specify modules as per your request, we also help companies establish their Document Management and technical writing system by guiding them with draft templates Required to prepare CTD’s.