Engy Aqladious

Experience acquired in Medical Devices demonstrated as follows; • Responsibility for importation and release approvals by preparing hard files, soft files and applying on Medevice. • QPPV, dealing with Pharmacovigilance department of medical devices, submitting files and following up the comments. • Responsible for Registration, Variation and Renewal files. • Dealing with NODCAR by submitting samples for analysis and the required paper. • Participation in external audits.

• Prepare and revise documents submitted to EDA. • Follow up the registration process and MOH Dr's Comments. • Preparation hard file for final revision.

• Dispensing prescription medicines and selling over-the-counter (OTC) drugs • Advising patients of any side effects or interactions with other medicines and/or food. • Improving customer service. • Training and supervision of pharmacy technicians.