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University of California, Irvine - Division of Continuing Education Online Certificate in Clinical Trials: Medical Device and Drug Development
University of California, Irvine - Division of Continuing Education

Online Certificate in Clinical Trials: Medical Device and Drug Development

USA Online, USA

12 up to 18 Months

English

Part time

Request application deadline

Jan 2025

USD 5,500 / per course *

Distance Learning

* average cost

Key Summary

    About: The Online Certificate in Clinical Trials: Medical Device and Drug Development focuses on the processes involved in clinical trials for medical devices and pharmaceuticals. This program helps you gain a solid understanding of regulatory frameworks, trial design, and data analysis. You'll explore crucial aspects of drug and device development in a flexible online format.
    Career Outcomes: Graduates can pursue roles in clinical research, regulatory affairs, and project management. Potential job titles include Clinical Research Coordinator, Regulatory Affairs Specialist, and Clinical Trials Manager. This certificate can enhance your career in the growing field of clinical trials.

Introduction

Overview

Demonstrating the effectiveness and safety of new medical products is a critical part of the medical product development process and requires significant resources to accomplish. Our program fills a growing need for professional learning that ensures designing and implementing clinical trials for success. The curriculum provides comprehensive knowledge of coordinating, monitoring and managing a clinical trial within a framework of good clinical practices and regulatory requirements. An internship course provides an invaluable capstone experience for the certificate.

Program Benefits

  • Gain the knowledge base needed to design and implement effective clinical trials.
  • Acquire a comprehensive knowledge of laws, regulations, guidance, and standard practices needed to surpass regulatory requirements
  • Improve time-to-market by applying approved clinical research regulations and clinical research guidelines
  • UCI Division of Continuing Education is a Regulatory Affairs Professional Society (RAPS) professional development provider
  • Earn credits to qualify for RAC recertification
  • Learn from instructors seasoned in practical industry experience who share their knowledge effectively
Read more on the institution's website

Curriculum

Ideal Students

English Language Requirements

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