/ http://www.slideshare.net/images/logo.gif / ºÝºÝߣShare feed for ºÝºÝߣshows by User: ravindrakullai https://cdn.slidesharecdn.com/profile-photo-ravindrakullai-48x48.jpg?cb=1571641915 • Regulatory affairs professional with 1.5 years of experience in registration of dossiers to Asia pacific and Gulf countries. • Having experience in compilation & submission of renewal dossiers to Asia Pacific and Gulf countries according to the format & guidelines issued by the respective drug regulatory authorities. • Compilation of renewal dossiers in ACTD and eCTD format. • Authoring the high quality CMC dossier sections as per country regulatory authority format. • Applying and tracking the CoPP, GMP and ML documents for renewal submissions. • Co-ordinate with various cross functional teams for documents, coll...