Omar Aljarallah Email & Phone Number

Saudi Arabia

• Ensuring the appropriate licensing of medical devices in order to control the safety and efficacy of products.
• Exhibiting extensive knowledge of medical device quality system regulation, and in-depth understanding of device safety requirements.
• Providing review and analysis of applicable regulatory guidelines and project regulatory assessments.
• Maintaining on-going surveillance and verification of the submitted document, ensuring compliance with relevant provisions of SFDA. Reviewing protocols and reports to support regulatory submissions.
• Propagating and conveying all necessary details/ procedures for evaluations and the standards to which such devices should conform. Ensuring the importers are registered in Medical Device National Registry, have.
• Maintaining pertinent medical device regulations to ensure submission are current, up-to-date, ensuring the imported medical device has obtained Medical Device Marketing Authorization and the manufacturer has an.

Saudi Arabia

year of training and practicing program through rotation in all sections of bio medical technology department.

Bachelor'S Degree, Biomedical/Medical Engineering

Bachelor'S Degree, Biomedical/Medical Engineering

- graduation project : measurement of the flexibility of removable partial denture.