Scientific office representative
Biologix
مجموع سنوات الخبرة :9 years, 5 أشهر
A.Follow-up products of the company after registering and marketing them as well as notifying SFDA immediately regarding any comments the quality and effectiveness of the product or the emergence of new side effects post marketing.
B. Follow-up the affairs of patents protection and manufacturing rights for products of the company.
C. Provide the accurate medicine information of company products that traded in the Kingdom for beneficiary and individuals working in the health and supervisory fields according to scientific bases.
D. Executing the regulations and instructions issued by Saudi Food and Drug Authority.
E. Make sure accuracy of information used in marketing for registered products of the company and its compatibility to Saudi Food and Drug Authority (SFDA) approved information.
F. Make sure the company's complies with the provisions of Saudi Arabian code of the ethics of pharmaceutical product marketing.
A. Prepare and update of the Pharmacovigilance system .
B. Preparation of safety reports .
C. Answers requests from National Pharmacovigilance Center (SFDA ) . D. Ongoing safety monitoring .
E. Contact point for Pharmacovigilance inspections .
F. Handling of any Emerging Safety Issues .
G. Detection any safety issues .
H. Submission documents to local authority .
I. Training AMCO employees for Pharmacovigilance .