Incepted in the year of 2015, Sarims Pharma is a company that brings together a number of experts in different segments of the pharmaceutical industry. Our area of expertise is the formulation process and documentation. We assist pharmaceutical laboratories for the realisation of their project and therefore we specialise in the sale of Dossier. Our experts work in synergy to achieve your performance.Sarims provides consulting and dossier solution for product registration. We write and review dossier as per European CTD / ASEAN CTD / non-CTD (country specific guideline).Administrative Documentation (writing and review):• Registration Application & Covering Letter• Letter of Authorisation• Legal & Administrative (GMP,CoPP, FSC etc) Documents• Summary of product (SmPC) and Pack Information Leaflet (PIL) or Pack insert• Label and carton contentsTechnical Documentation (writing and review):• Summaries – Quality & Non-clinical• Drug master file (S Part of Dossier)• Non-clinical Overview (Module 2)• PDR, Process validation, AMV & Stability Studies• Specification, Method of analysis & Certificate of Analysis of Raw materials & Packing Materials• Specification, Method of analysis & Certificate of Analysis of Formulation product• Module 4 (Non-clinical)• Module 5 (Non-clinical)