Medical Devices

Targeted knowledge to enter new markets and build a stronger quality culture.

Medical Devices


Libraries organize courses by subject matter, featuring expert regulatory interpretation by company specialists, industry leaders and key government agencies.

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  • Clinical - Medical Device Library

    Clinical - Medical Device

    This online library, specifically targeted to the Medical Device industry, covers underlying Good Clinical Practice (GCP) concepts as well as specific, advanced information for clinical professionals based on their role in the study.

    21 courses

  • Engineering Safety Library

    Engineering Safety

    In this online library, you will be introduced to the ISO and IEC standards that impact the development and approval of medical device products, including IEC 60601, ISO 14971 among others.

    7 courses

  • Ethics and Corporate Responsibility Library

    Ethics and Corporate Responsibility

    In this eLearning library, you will have access to several Code of Conduct online training courses designed to teach you about ethics and corporate responsibility.

    38 courses

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Medical Devices


Programs address specific industry needs by offering individual course combinations in convenient packages.

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  • Computer Systems Validation Program

    Computer Systems Validation

    Learn to meet the FDA’s computerized systems compliance regulations while managing validation activities and reducing validation requirements.

    6 courses

  • HR Compliance Program

    HR Compliance

    A program designed to address compliance and risk management issues while helping HR professionals improve workplace performance.

    5 courses

  • Medical Device GMP Program

    Medical Device GMP

    Achieve regulatory compliance as specified in the Quality System Regulation (QSR) with UL’s Medical Device GMP program.

    5 courses

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Medical Devices


Written and reviewed by subject matter experts, our courses are regularly updated to reflect the most current expectations and requirements of regulators and industry groups.

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  • Basics of the AdvaMed Code

    Basics of the AdvaMed Code

    Your team will learn the basics of the AdvaMed code and how it impacts interactions with health care professionals.

  • Essentials of an Effective Calibration Program

    Essentials of an Effective Calibration Program

    Proper calibration protects against major injuries and class action lawsuits. This course provides the tools you need to create an effective system for equipment calibration.

  • QSIT 3: The Design Controls Subsystem

    QSIT 3: The Design Controls Subsystem

    In this third of five courses on QSIT, your team will learn to identify the inspectional objectives associated with the design control system and determine methods to accomplish the objectives.

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