Shahriar Arbabi

Led reviews for Class II & III medical devices for EU-MDR submissions, assessing compliance requirements and evaluating supportive documents. Conducted data analysis from clinical studies and maintained up-to-date knowledge of regulatory guidelines.

Authored clinical evaluation plans and reports for EU-MDR submission, conducted systematic literature reviews, and managed multiple writing projects ensuring timely submissions. Collaborated with cross-functional teams.

Designed scientific research plans for clinical studies, secured regulatory approvals, and monitored trial operations. Prepared clinical study reports and facilitated scientific meetings with stakeholders.

Authored clinical trial protocols and informed consent documents, contributed to regulatory submissions, and monitored study progress. Ensured data accuracy and participant safety.

Contributed to fetal surgery research and participated in educational initiatives. Supported multiple clinical research projects.

Provided training to healthcare professionals and specialized in pediatric anesthesiology. Managed clinical trials and contributed to hospital committees.

Delivered anesthesia care to patients and oversaw post-operative care. Contributed to staff recruitment and training.

Completed a Master's in Public Health with a focus on Healthcare Management, equipping me with the skills to analyze and improve health systems and policies.

Achieved a Master's in Healthcare Administration (MBA), focusing on the business aspects of healthcare delivery and management.

Completed a residency in Anesthesiology and Critical Care, gaining extensive clinical experience in anesthesia practices and patient management.

Earned a Doctor of Medicine degree, providing a comprehensive foundation in medical sciences and clinical practices.