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Good Documentation Practices - July 30, 2024

Started Apr 18, 2024


Full course description

This course will cover various methods for documenting accurately and thoroughly the observations and requirements for clinical research studies.

Learning Objectives:

- Define ALCOA
- State the events that require prompt reporting to the IRB
- Identify consent DOs and DON'Ts
- Describe good time management for maintaining study records.

Speaker: Peg Tsao, RN, CCRC, Manager, Workforce Development, Spectrum

Date:               Tuesday July 30th, 2024
Time:               9:30 - 11:00 AM
Location:         Zoom / Virtual Seminar. After enrolling, return to the course website to obtain the zoom link. This class will be held LIVE on the date above.

Certificate Program: CORE
Competency: Clinical Trial Operations

Target Audience: Research coordinators, nurses, faculty, staff and post-doctoral scholars working on clinical research projects at Stanford University. 

Spectrum is an approved provider by the California Board of Registered Nursing, Provider Number CEP15435 for 1.5 contact hour(s). If you would like to receive credit for attending this class, on the evaluation, please  enroll here: and add your employee ID and acknowledge fee on evaluation. A $35 administrative fee will be charged to your STAP. You will be required to complete the quiz and evaluation before receiving your certificate of attendance. 

BRN CANCELLATION POLICY: If you need to cancel, please do so within 24 hours of the course date or notify to receive a refund.

Sign up for this course today!