A self motivated, hard 颅 working and technically sound professional, with a combined industrial experience of 9 years in Drug Regulatory Affairs, Quality Assurance, Validations, Qualifications and Trainings.
Highlights:
鈥� Expertise in writing and reviewing CTD Modules, DMF, compliance reports, SOPs, Stability Protocols, Change Control, Deviations, equipments, systems qualification and/or validation protocols etc.
鈥� Well versed with current drug regulatory and cGMP requirements as per different regulatory guidelines e.g. ICH, US FDA, EMA, WHO, MHRA, TGA etc.
鈥� A connecting Trainer: Conducted training sessions in companies and institutes on topics viz. Common Technical Documents (CTD)...
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