CRA Curriculum

Online Clinical Courses can be purchased for $175 each. Once your purchase is complete, you will receive an e-mail with instructions on how to take your course.

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Course Listing

GCP/ICH Obligations of Sponsors, Monitors, and Investigators

This course addresses the obligations of sponsors, monitors, and investigators who conduct and verify clinical research that is governed by US FDA regulations and ICH guidelines. ACPE Universal Program Number: 234-000-04-002-L04; California Board of Nursing Program Number: 47111-2004-CBT-198 — (1.5 Contact Hours/Credits)

GCP Obligations of Sponsors and Monitors

This course addresses the obligations of sponsors and monitors who conduct and verify clinical research that is governed by US FDA regulations and ICH guidelines. ACPE Universal Program Number: 234-000-04-004-L04; California Board of Nursing Program Number: 47111-2004-CBT-199 — (1.5 Contact Hours/Credits)

Obligations of Investigators in Conducting Drug and Biologic Trials

This course addresses investigator requirements and responsibilities for the conduct of clinical trials in support of new drug and biologics applications. ACPE Universal Program Number: 234-000-04-001-L04; California Board of Nursing Program Number: 47111-2004-CBT-200 — (1.5 Contact Hours/Credits)

Obligations of Investigators in Conducting Medical Device Trials

This course addresses investigator requirements and responsibilities for the conduct of clinical trials in support of new medical device applications. ACPE Universal Program Number: 234-000-04-003-L04; California Board of Nursing Program Number: 47111-2004-CBT-201 — (1.5 Contact Hours/Credits)

Ethical Review Boards

This course covers IRB/IEC members, investigators, and sponsors/CROs obligations in relation to the IRB/IEC and will be able to ensure that policies and procedures developed for compliance will protect and safeguard the research subjects. ACPE Universal Program Number: 234-000-04-007-L04; California Board of Nursing Program Number: 47111-2004-CBT-208 — (2 Contact Hours/Credits)

Informed Consent

This course will introduce you to informed consent regulations and guidelines, the informed consent process, and the roles and responsibilities of clinical research professionals in ensuring the protection of human subjects through the informed consent process. ACPE Universal Program Number: 234-000-04-016-L04; California Board of Nursing Program Number: 47111-2004-CBT-207 — (2 Contact Hours/Credits)

Drug Safety and Adverse Event Reporting

This course will introduce you to the regulatory requirements in the clinical trial and post-marketing environments, as well as educate you on drug safety monitoring efforts internationally. ACPE Universal Program Number: 234-000-04-014-L04; California Board of Nursing Program Number: 47111-2004-CBT-209 — (2 Contact Hours/Credits)

Ethics as the Foundation of Clinical Research

This course examines current ethical issues in clinical research with a focus on ethical principles in historical and current regulations. ACPE Universal Program Number: 234-000-04-015-L04; California Board of Nursing Program Number: 47111-2004-CBT-210 — (1 Contact Hour/Credit)

The Role of The Clinical Research Associate

This course discusses the role of the CRA in regards to clinical operations and monitoring activities. ACPE Universal Program Number: 234-000-04-009-L04; California Board of Nursing Program Number: 47111-2004-CBT-211 — (2 Contact Hours)

Continuing Nursing Education The California Board of Registered Nursing approves the Association of Clinical Research Professionals (ACRP) as a provider of continuing nursing education. Program Numbers 47111-2004-CBT-198 through 47111-2004-CBT-213). Continuing Pharmacy Education The Association of Clinical Research Professionals is accredited by the Accreditation Council on Pharmacy Education as a provider of continuing pharmacy education. ACPE Universal Program Numbers 234-000-04-001-L04 through 234-000-04-016-L04