Good Documentation Practices (GDP) for the Medical Device Industry

At the end of this short course, successful learners will be able to:

• Explain what GDP is and why it is critical for regulatory compliance in the medical device industry
• Apply the ALCOA+ principles
• Recognize common errors and pitfalls in documentation and how to avoid them
• Demonstrate correct practices for creating, reviewing, approving, and storing documentation
• Understand the regulatory expectations of authorities

This course is for individuals or organizations who want to understand Good Documentation Practices (GDP) in the medical device industry.

Successful completion of the course examination will entitle each Learner to receive a digital Certificate of Completion.

In order to successfully complete this course, each Learner will need to:

• Complete all eLearning modules and obtain 70% or higher in the final assessment (MCQ-based)

There are recommended requirements for each Learner in wishing to complete any of our eLearning modules. In our experience, Workplace IT environments’ internal configurations and available software can vary (new or old), and there may be various limitations or other restrictions in place, and as such, the functionality of any Learning Management System (LMS) may be impacted, restricted and may not perform well. Read the full technology requirements here.