Online Learning Center

• On-demand training courses — access anytime, anywhere you have an internet connection for up to 1 year from date of purchase
• Learn at your own pace
• Interactive course includes interspersed review questions, and a quiz at the end of each module
• Certificates of completion are available
• RQAP re-registration units are available for individual courses

Bulk Pricing: If you are interested in buying five or more online learning programs (five instances of one course for your staff, five separate courses for yourself, or any combination thereof), please download our Online Learning Bulk Order Form.


Access Online Education That I Ordered

 

Now Available! GLP Study Director and Principal Investigator Training Format: Interactive Training Course delivered on-demand in 7 modules RQAP re-registration credit:  1.5 GLP or non-GCP units This course, brought to you by the SQA Learning Foundation, is for individuals who are new to, or in training for, the role of Study Director or Principal Investigator or those who are seeking a comprehensive refresher of what it means to be the single point of GLP study control and study/study phase direction. The course will provide a thorough overview of the regulatory requirements for study oversight and direction and the roles and responsibilities of GLP Study Directors and Principal Investigators. Buy Now!

Good Clinical Practice: Understanding the Basics Format: Interactive Training Course delivered on-demand in 14 modules RQAP re-registration credit:  2.69 GCP or non-GLP units for completion of all 14 modules This course, brought to you by the SQA Learning Foundation, is for GCP auditors with zero to one year of experience and anyone who would like to learn the basics of GCP. It is designed to provide an overview of the fundamentals of Good Clinical Practice. Some applied knowledge is required to work through interactive review questions and quizzes, but advanced concepts are not within the scope of this training. This ICH E6 GCP Investigator Site Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma Inc. as necessary to enable mutual recognition of GCP training among trial sponsors. Try Module 1 of the Course for FREE! Buy Now!

Basic Training: Good Laboratory Practice Format: Interactive Training Course delivered on-demand in 11 modules RQAP re-registration credit:  3.38 GLP or non-GCP units for completion of all 11 modules This course, brought to you by the SQA Learning Foundation, is designed for anyone needing to learn about GLP regulations, including, but not limited to: QA Personnel (GLP Auditors), Study Directors, Principal Investigators, Management, Scientists, Technicians, Facilities Personnel, and Archivists, with 0 to 2 years or more of experience. Some applied knowledge is required to work through interactive review questions and quizzes, but advanced concepts are not within the scope of this training. Try Module 1 of the Course for FREE! Buy Now!

Introduction to 21 CFR Part 11: Electronic Records; Electronic Signatures Format: Interactive Training Course delivered on-demand in 1 module RQAP re-registration credit:  0.29 GLP or non-GCP This course, brought to you by the SQA Learning Foundation, is for Quality Assurance professionals, IT, business system owners, and management who use GxP-validated systems and would benefit from an introduction to the principles of 21 CFR Part 11. It is is an introductory course that explains the contents of 21 CFR Part 11 (Electronic Records; Electronic Signatures), including the scope, Parts, and definitions of the key terms used in Part 11, and provides real-life examples of how to apply Part 11 principles. Buy Now!

Introduction to Writing Effective Compliant GLP SOPs Format: Interactive Training Course delivered on-demand in 1 module RQAP re-registration credit:  0.25 GLP or non-GCP This course, brought to you by the SQA Learning Foundation, is for GLP auditors from novice to experienced. It is designed to familiarize the trainee with the GLP requirements for SOPs. It will provide a review of common 483s for missing or ineffective SOPs, as well as industry guidance for SOP management. The course will also review SOP lifecycle and distribution. In addition, it will provide technical writing tips to enable the trainee to write and/or review SOPs for increased effectiveness. Finally, it will enable the trainee to perform an audit of an SOP process. Buy Now!

An Introduction to Basic Pharmacovigilance Requirements, Concepts and Processing for Quality Professionals This course has been decommissioned by SQA due to its age. The SQA Pharmacovigilance Specialty Section and the SQA Learning Foundation Board of Directors are working on a plan to produce an updated online pharmacovigilance course. If you purchased this course within the past year, you still have access to the materials via the SQA Online Learning Center. The course is only closed to new enrollments.