eLearning - Medical Device RA/QA

Leverage ELIQUENT Life Sciences’s eLearning development capabilities to enhance your organization’s RA/QA learning and development program.

Our team will work with you to identify your needs and provide the right eLearning solution to meet your organization’s requirements. Select from a library of foundation and awareness modules covering important topics like FDA’s QSR, ISO 13485, MDSAP, EU Medical Device Regulation (MDR), EU In Vitro Diagnostic Regulation (IVDR), risk management, root cause investigation, document control, and clinical evaluation. Alternatively, we can work with you to develop a unique eLearning program that meets the specific needs of your organization.

Benefits of eLearning solutions from ELIQUENT Life Sciences:

• Proven, up-to-the-minute content sourced from the largest library of RA/QA learning assets in the medical device industry
• All the benefits of eLearning – anyone, anytime, anywhere
• Instructional design and development experts utilizing current authoring tools and techniques – seamless integration with today’s learning management system platforms
• Design strategies to achieve learning and business outcomes, corporate-wide initiatives, and just-in-time and blended learning solutions
• Rapid development methods that enable quick and effective customization of content
• Objective-based assessments that provide evidence that learners have mastered the desired content

Why choose ELIQUENT Life Sciences?

Since 1968, ELIQUENT Life Sciences has been an industry leader in RA/QA training. Our medical device course library covers a broad range of topics, is always up to date with the most current regulations, and is designed by experienced instructional designers to ensure an optimal learning event.