I am a regulatory affairs pharmacist with more than 8 years experience in regulatory affairs. Having a good knowledge of the local pharma environment, I can support and represent companies in Algeria for several roles pré and post registration activities for both pharmaceutical drugs and medical devices , such as: Preparing a detailed market study (to) estabilishing a Regulatory strategy planning - (to) - Pre-market application preparation and submission To registration (new and renewals) at the local Health authorities, and pricing, including also labelling, writings - (to) - market authorization - (to) - commercialization - (to) - Post-market total product lifecycle management - Technology/Product approvability evaluation for technical and regulatory due diligence including regulatory requirement review. - Correspondence with regulatory authorities . I can also help wih submission To local tenders, writing SOPs, preprartion CTDs ...etc I also translations from and into arabic-french-english.