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Clinical Trials & Regulatory Affairs

Get the training to conduct clinical trials and fulfill the educational requirements to become a CRA or CRC.

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Join the thriving clinical trials market

Conducting clinical trials is essential to ensure the safety and efficacy of new drugs, biologics and medical devices. The demand for highly trained professionals to coordinate and manage clinical trials for the local, national and international biomedical and biotech communities continues to grow rapidly. By learning key concepts, guidelines, regulations and best practices, professionals gain the skills needed to become part of an active workforce and fulfill the requirements to become a CRA or CRC through ACRP, or CRP through SoCRA.

Two Clinical Trials Certificates - What are the differences?
Certificate

Two Clinical Trials Certificates - What are the differences?

Two top-rated training programs developed by leaders in the biomedical research industry - choose the one right for you. Gain an overview of the entire clinical research process to identify the various career paths within the industry.

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Regulatory Affairs for Medical Devices
CERTIFICATE

Regulatory Affairs for Medical Devices

Develop the skills to ensure that quality and compliant medical devices get to the patients who need them most.

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Clincial Trials in Oncology
Understanding Oncology

Clincial Trials in Oncology

Through a series of web-based sessions, students will learn pathology, diagnostics and disease management.

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