• OnDemand Notice


    ON DEMAND NOTICE

    ​This site is no longer in-service to purchase courses. You may still access and complete training.

     

    Please visit our PureSafety OnDemand site to access our latest eLearning training offerings: https://ondemand.puresafety.com/

  • GMPs: Dietary Supplements


    This six-course series focuses on US FDA's GMP regulations (Part 111) for dietary supplements. The US FDA expects dietary supplement manufacturers to implement production process controls, a quality control department, a customer complaint system, documented testing, batch and laboratory records maintenance and change controls.

  • Medical Device GMPs


    Provide convenient online learning to manufacturing and production teams. Our GMP courses focus on key sections of FDA's QSR regulations (21 CFR Part 820), QSIT inspections and much more.

  • FDA Medical Device Reporting (MDR) Series


    The FDA-Authored MDR Course Series, part of the FDA Inspection and Enforcement Library, focuses on the Medical Device Reporting (MDR) regulation, which provides one mechanism for the Food and Drug Administration (FDA) and manufacturers to identify and monitor significant adverse events involving medical devices. The goal of the regulation is to detect and correct product problems in a timely manner.

  • Pharmaceutical GMPs


    Hundreds of pharmaceutical, biotechnology and biologic facilities worldwide rely on UL to assure regulatory compliance, product safety and workforce productivity in a fast-changing global economy. 

    The same technology and curricula used by FDA are available exclusively to UL’s clients. 

  • Medical Device Packaging, Labeling and Distribution Requirements


    Help your manufacturing team understand US FDA's QSR packaging and labeling requirements (21 CFR Part 820, Subpart L and K, 21 CFR Part 801).
2.8.3.11

OSHA and Safety Online Courses 

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