/ http://www.slideshare.net/images/logo.gif / ºÝºÝߣShare feed for ºÝºÝߣshows by User: SwatiSuhag https://cdn.slidesharecdn.com/profile-photo-SwatiSuhag-48x48.jpg?cb=1527779787 QA/RA Associate having experience in Quality Assurance & Regulatory Affair within pharmaceutical industry as per GMP, CTD, ACTD and eCTD ,GCP along with drug registration experience with international drug & health regulatory bodies. Skills & interest • Good communication & presentation skills • Team player with good interpersonal skills • MS office, Internet & Adobe • eCTD submission (Lorenz docubridge software tools) • EDC submission (Medrio and Medidata Rave systems)-edit check & data entry • Quality assurance, Regulatory Affair & Clinical Trials documentation • GMP (21 CFR 210,211, 820), GCP, Drug Labeling • Event organization Certifications :Registered Pharmacist (India), Communi...