Responsible for preparation of Registration dossiers of all new products and Re-registered products. Submitting variations of existing products. Responsible for preparation and submission of Analytical dossiers to NODCAR ( National Organization for Drug Control and Research ). Follow up submission and any supporting documents along with registration lead time. Support logistic team with all references, legalized certificates and material needed for regular analysis and release. Prepare analytical files to be submitted to different authorized labs Follow up analysis and supply all needed requirements to get release certificates f samples. Ensures confidentiality in respect of registration files contents. Completing all registration requirements for all shipments at EDA. Responsible for obtaining Ministry of Health importation approvals, inspection & release.