Welcome to the Ampin's PharmaHave a very Good Day...............☻️Ampin's Pharma comprises a group of experienced regulatory affairs consultants specialising in Pharmaceutical & Medical Device Regulatory Affairs with highly skilled in Dossiers compilation to the global regulatory authorities at CTD, eCTD, ACTD & Country specific formats for the CIS Countries, ASEAN, AFRICAN, Middle East, Latin American (Latam) & the ROW Markets. We are supporting Pharma and Healthcare industries for Regulatory framework in their entire Regulatory chain ranging from Regulatory Strategy, Intelligence, Dossiers, Submissions etc to Post- Approval, Product Maintenance, Query resolve, Artwork Management and other related functions. We are an effective solution for both your short and long-term regulatory or compliance requirements. Our services include (but not limited to):● CTD Dossiers Compilation ● eCTD Dossiers Compilation ● ACTD Dossiers Compilation ● Country Specific Dossiers ● CTD DMF Services ● eCTD DMF Services ● BE/BA Study ● Artwork Management ● Query Resolvation ● Site Master Files (SMF)● Process validation Report (PV)● Product Development Report (PDR)● Analytical Method Validation (AMV)● Comparative Dissolution Profile (CDP)● Periodic safety update report (PSUR)● Risk Management Plan (RMP)● Stability Study Reports Currently we are working with the various small to large scale companies by giving our regulatory services for obtaining  approval or registration of their products into the Global Markets and we are very excited to Serve you & your Organisation..!