/ http://www.slideshare.net/images/logo.gif / ºÝºÝߣShare feed for ºÝºÝߣshows by User: anuradhasingh12327 https://cdn.slidesharecdn.com/profile-photo-anuradhasingh12327-48x48.jpg?cb=1594386924 A self motivated, hard ­ working and technically sound professional, with a combined industrial experience of 9 years in Drug Regulatory Affairs, Quality Assurance, Validations, Qualifications and Trainings. Highlights: • Expertise in writing and reviewing CTD Modules, DMF, compliance reports, SOPs, Stability Protocols, Change Control, Deviations, equipments, systems qualification and/or validation protocols etc. • Well versed with current drug regulatory and cGMP requirements as per different regulatory guidelines e.g. ICH, US FDA, EMA, WHO, MHRA, TGA etc. • A connecting Trainer: Conducted training sessions in companies and institutes on topics viz. Common Technical Documents (CTD)... http://www.machlibazar.com/blog