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Able to expedite the documents required by Latin America BoH. Knowledge of the different sections (CTD) that have direct impact on the product. Knowledge of Latin America regulations relative to pharmaceutical and nutritional products. Capable of preparing documents for registration, variations and product renewals.. Knowledge of Good Documentation Practices. Able to expedite legal documents that make up a dossier. Evaluati...
Professional Summary Regulatory affairs associate adept in research and documentation of product dossier. Provide clear and concise information based on creative and complex findings. Also a dedicated lecturer with a stong work ethic. Skillfully manages lectures and promotes open classroom discussions. Regulatory affairs associate Jan 2011 - Feb 2012 Alice Pharma Pvt Ltd Mumbai, India * Regulatory Dossiers Preparation. * Co...
I hope to expand my role as a regulatory/research study coordinator in a thriving academic or pharmaceutical setting.
Regulatory Affairs professional seeking to change industries for petrochemical regulatory matters to biotech and medical device industry. Proven aptitude to in dealing with regulatory authorites with special expertise in the Asia Pacific region.