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Master list of training

  • FDA/CGMP Medical Devices Executive Overview & Management Review for meeting FDA requireme in Spanish
  • FDA/CGMP Medical Devices Executive Overview & Management Review for meeting FDA requirements Chinese
  • FDA/CGMP Medical Devices Executive Overview & Management Review for meeting FDA requirements
  • FDA/CGMP Medical Devices Introduction & Employee Overview in Spanish
  • FDA/CGMP Medical Devices Introduction & Employee Overview in Chinese
  • HACCP Introduction & Employee Overview
  • FDA/CGMP Medical Devices Introduction & Employee Overview
  • Quality Improvement Concepts -continuous improvements-problem solving and customer satisfaction
  • FDA/CGMP for Medical Devices, Auditing/ Auditor/Implementation in Spanish
  • FDA/CGMP for Medical Devices, Auditing/ Auditor/Implementation in Chinese
  • HACCP Audting and Implementation in Chinese
  • Business Continuity/Contingency Planning Implementation and Auditing/Auditor
  • Injury and Illness Prevention Plan Implementation and Auditing/Auditor
  • Storm Water Pollution Prevention Implementation & Auditing/Auditor
  • Respiratory Planning - Implementation and Auditing/Auditor
  • Lockout/Tagout Plan - Implementation and Auditing /Auditor
  • FMEA, Risk Analysis for Medical Devices
  • FMEA, Potential Failure Mode Effect Analysis
  • HACCP Seafood - Implementation & Auditing/Auditor
  • FDA/CGMP Food - Implementation & Audit/Auditor
  • FDA/CGMP Blood - Implementation & Audit/Auditor
  • HACCP Implementation and Auditing/Auditor
  • FDA/CGMP for Medical Devices, Auditing/ Auditor/Implementation
  • ESD EMPLOYEE AWARENESS
  • ESD Overview, Implementation and Auditing /Auditor
  • 8 D Problem Solving Methodology, Corrective Action, and Good Business Practices
  • FDA-GMP Good Laboratory Practice for nonclinical (21 CFR part58) Implementation and Auditing.
  • FDA/CGMP Drug (Pharmaceutical) - Implementation and Audit/Auditor (21CFR210-211)
  • CE Marking (90/385) for Active Implantable Medical Devices- Essential Requirements Only
  • CE Marking (90/385) for Active Implantable Medical Devices- Implementation and Auditing
  • CE Marking (93/42 ECC) for medical devices- Essential Requirements only
  • CE Marking (93/42 ECC) for medical devices- Implementation and Auditing
  • CE Marking IVD 98-79 EEC Implementation and Auditing, Essential Requirements Only
  • CE Marking IVD 98-79 EEC Implementation and Auditing
  • Dietary Supplements: Overview Based on FDA Guidance 2002
  • TL 9000: Internal Auditing
  • ISO 9001:2000 Internal Auditing/Auditor and Implementation
  • ISO 9001:2008: Introduction & Awareness for meeting ISO 9001 requirements
  • ISO 9001:2008: Executive and Management Review for meeting ISO 9001:2008 requirements
  • ISO 9001:2008 Internal Auditor and Implementation
  • ISO 9001 Executive and Management Review for meeting ISO 9001 in Spanish
  • ISO9001 Introduction and Awareness for meeting ISO 9001 in Spanish
  • ISO 9001 Capacitación del Auditor Interno in Spanish
  • ISO 9001:2000: Executive and Management Review for meeting ISO 9001:2000 requirements
  • ISO 9001:2000: Introduction & Awareness for meeting ISO 9001 requirements
  • AS 9100 Rev B Internal Auditing/Auditor and Implementation
  • AS 9100 Rev C: Executive and Management Review for meeting AS 9100 requirements
  • AS 9100 Rev C: Introduction & Awareness for meeting AS 9100 requirements
  • AS9100 Rev C Internal Auditor and Implementation
  • AS 9100 Rev B: Executive and Management Review for meeting AS 9100 requirements
  • AS 9100 Rev B: Introduction & Awareness for meeting AS 9100 requirements
  • ISO 13485 Internal Auditing/Auditor and Implementation in Chinese
  • ISO 13485: Internal Auditing /Auditor and Implementation
  • ISO 13485 Executive Management Review meeting ISO 13485
  • ISO 13485: Introduction & Awareness for meeting ISO 13485 requirements
  • ISO 14001 Internal Auditing/Auditor Implementation in Chinese
  • ISO 14001:2004 Internal Auditing/Auditor and Implementation
  • Aspect, Significant Impact Process/Calculation Method for meeting ISO 14001
  • Environmental, Health and Safety Training for meeting DOT, ISO 14001, OSHA, OSHA 18001,.........
  • ISO 14001:2004 Executive Review & Management Review for meeting ISO14001
  • ISO 14001:2004 Introduction & Awareness for meeting ISO 14001 requirements
  • RISK Management Employee Overview for Medical Device meeting ISO 14971/ISO 13485/FDA/CE MARK
  • ISO 14971 Risk Management Implementation & Auditing/Auditor meeting FDA /ISO13485/CE Marking
  • ISO/TS 16949 INTERNAL AUDITING/AUDITOR and IMPLEMENTATION
  • ISO/TS 16949: Executive Review & Management Review for meeting ISO/TS 16949 requirements
  • ISO/TS 16949 Introduction & Awareness for meeting ISO/TS 16949 requirements
  • ISO 17025 Internal Auditing/ Auditor and Implementation Training
  • ISO 17025 Introduction and Employee Overview
  • ISO 17025 Executive Management Overview
  • OHSAS 18001: Introduction and Employee Overview
  • Safety Risk Assessment, Calculation Method, Hazard Identification, and Risk Control for OSHA 18001
  • >- Hazard ManagementTraining for meeting DOT, OSHA, OSHA 18001, ISO 14001, HACCP..............
  • Hazard Communication Training for meeting DOT, OSHA, OSHA 18001, ISO 14001, HACCP..
  • OHSAS 18001: Executive & Management Overview
  • OHSAS 18001: Internal Auditing/Auditor and Implementation
  • ISO 20000 (Information technology: Service management): Internal Auditing/Auditor and Implementation
  • ISO 22000 Food safety management systems: Internal Auditor/Auditing training and implementation
  • ISO 27001 Information Security Management: Internal Auditing Training and Implementation

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    Quality University, Inc. provides convenient learning formats and options to serve professionals, companies, and individuals who wish to obtain and/or maintain certification, advance in their careers, change professions, or update their knowledge and skills. You can take training at your own pace. You can logon and logout as many times as needed. You can re-take the exam as many times as necessary until you pass the exam and an online certificate is issued.

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       - Xincai Qiao, JCP Marine Pte Ltd, Singapore

     

    "Ease of use was excellent. It was really convenient for me. I could do it on my own time after work. I liked how you could follow the question through the chapters."

    - Nathan Williams, FedEx

     

    "The website is easy to use and re-use.  I liked the fact that I could work at my pace and leave and return as needed throughout my workday.  The course was complete and concise, everything was easy to find and use."

      - James Hutchinson, American Medical Systems

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    TRAINING BY STANDARD

    TRAINING BY PROCESS

    ISO 9001

    Test Lab

    ISO 14971

    Employee

    ISO 22000

    Internal Auditor

    ISO 20000

    Management

    ISO 17025

    Automotive

    ISO 27001

    OHSAS

    ISO 13485

    Environment

    ISO 14001

    Food Safety

    TS 16949

    Calibration Lab

    TL 9000

    Respiratory Planning

    AS 9100

    Safety Risk Assessment

    OHSAS 18001

    Risk Management

    HACCP

    Health and Safety

    ESD

    8 D Problem Solving

    FMEA

    Lockout/Tagout Plan

    FMEA for Medical Devices

    Hazard Communication

    FDA/CGMP

    Injury and Illness Prevention

    FDA/CGMP Blood

    Information Technology

    FDA/CGMP Food

    Food Safety Management

    FDA/CGMP Drugs (21 CFR 210-211)

    Quality Improvement Concepts

    FDA/CGMP Nonclinical (21 CFR Pt. 58)

    Environmental Health and Safety

    CE Marking IVD 98/79

    Storm Water Pollution Prevention

    CE Marking 90/385/EEC

    Information Security Management

    CE Marking 93/42/EEC

    Business Continuity/ Contingency Planning

    Quality University mark is a registered trademark of Quality University and should not be used by any person or company without written approval from Quality University.

    Master List of Online Training >>
    Training by Standard:
    FDA/CGMP Medical Devices Executive Overview & Management Review for meeting FDA requireme in Spanish

    FDA/CGMP Medical Devices Executive Overview & Management Review for meeting FDA requirements Chinese

    FDA/CGMP Medical Devices Executive Overview & Management Review for meeting FDA requirements

    FDA/CGMP Medical Devices Introduction & Employee Overview in Spanish

    FDA/CGMP Medical Devices Introduction & Employee Overview in Chinese

    HACCP Introduction & Employee Overview

    FDA/CGMP Medical Devices Introduction & Employee Overview

    Quality Improvement Concepts -continuous improvements-problem solving and customer satisfaction

    FDA/CGMP for Medical Devices, Auditing/ Auditor/Implementation in Spanish

    FDA/CGMP for Medical Devices, Auditing/ Auditor/Implementation in Chinese

    HACCP Audting and Implementation in Chinese

    Business Continuity/Contingency Planning Implementation and Auditing/Auditor

    Injury and Illness Prevention Plan Implementation and Auditing/Auditor

    Storm Water Pollution Prevention Implementation & Auditing/Auditor

    Respiratory Planning - Implementation and Auditing/Auditor

    Lockout/Tagout Plan - Implementation and Auditing /Auditor

    FMEA, Risk Analysis for Medical Devices

    FMEA, Potential Failure Mode Effect Analysis

    HACCP Seafood - Implementation & Auditing/Auditor

    FDA/CGMP Food - Implementation & Audit/Auditor

    FDA/CGMP Blood - Implementation & Audit/Auditor

    HACCP Implementation and Auditing/Auditor

    FDA/CGMP for Medical Devices, Auditing/ Auditor/Implementation

    ESD EMPLOYEE AWARENESS

    ESD Overview, Implementation and Auditing /Auditor

    8 D Problem Solving Methodology, Corrective Action, and Good Business Practices

    FDA-GMP Good Laboratory Practice for nonclinical (21 CFR part58) Implementation and Auditing.

    FDA/CGMP Drug (Pharmaceutical) - Implementation and Audit/Auditor (21CFR210-211)

    CE Marking (90/385) for Active Implantable Medical Devices- Essential Requirements Only

    CE Marking (90/385) for Active Implantable Medical Devices- Implementation and Auditing

    CE Marking (93/42 ECC) for medical devices- Essential Requirements only

    CE Marking (93/42 ECC) for medical devices- Implementation and Auditing

    CE Marking IVD 98-79 EEC Implementation and Auditing, Essential Requirements Only

    CE Marking IVD 98-79 EEC Implementation and Auditing

    Dietary Supplements: Overview Based on FDA Guidance 2002

    TL 9000: Internal Auditing

    ISO 9001:2000 Internal Auditing/Auditor and Implementation

    ISO 9001:2008: Introduction & Awareness for meeting ISO 9001 requirements

    ISO 9001:2008: Executive and Management Review for meeting ISO 9001:2008 requirements

    ISO 9001:2008 Internal Auditor and Implementation

    ISO 9001 Executive and Management Review for meeting ISO 9001 in Spanish

    ISO9001 Introduction and Awareness for meeting ISO 9001 in Spanish

    ISO 9001 Capacitación del Auditor Interno in Spanish

    ISO 9001:2000: Executive and Management Review for meeting ISO 9001:2000 requirements

    ISO 9001:2000: Introduction & Awareness for meeting ISO 9001 requirements

    AS 9100 Rev B Internal Auditing/Auditor and Implementation

    AS 9100 Rev C: Executive and Management Review for meeting AS 9100 requirements

    AS 9100 Rev C: Introduction & Awareness for meeting AS 9100 requirements

    AS9100 Rev C Internal Auditor and Implementation

    AS 9100 Rev B: Executive and Management Review for meeting AS 9100 requirements

    AS 9100 Rev B: Introduction & Awareness for meeting AS 9100 requirements

    ISO 13485 Internal Auditing/Auditor and Implementation in Chinese

    ISO 13485: Internal Auditing /Auditor and Implementation

    ISO 13485 Executive Management Review meeting ISO 13485

    ISO 13485: Introduction & Awareness for meeting ISO 13485 requirements

    ISO 14001 Internal Auditing/Auditor Implementation in Chinese

    ISO 14001:2004 Internal Auditing/Auditor and Implementation

    Aspect, Significant Impact Process/Calculation Method for meeting ISO 14001

    Environmental, Health and Safety Training for meeting DOT, ISO 14001, OSHA, OSHA 18001,.........

    ISO 14001:2004 Executive Review & Management Review for meeting ISO14001

    ISO 14001:2004 Introduction & Awareness for meeting ISO 14001 requirements

    RISK Management Employee Overview for Medical Device meeting ISO 14971/ISO 13485/FDA/CE MARK

    ISO 14971 Risk Management Implementation & Auditing/Auditor meeting FDA /ISO13485/CE Marking

    ISO/TS 16949 INTERNAL AUDITING/AUDITOR and IMPLEMENTATION

    ISO/TS 16949: Executive Review & Management Review for meeting ISO/TS 16949 requirements

    ISO/TS 16949 Introduction & Awareness for meeting ISO/TS 16949 requirements

    ISO 17025 Internal Auditing/ Auditor and Implementation Training

    ISO 17025 Introduction and Employee Overview

    ISO 17025 Executive Management Overview

    OHSAS 18001: Introduction and Employee Overview

    Safety Risk Assessment, Calculation Method, Hazard Identification, and Risk Control for OSHA 18001

    >- Hazard ManagementTraining for meeting DOT, OSHA, OSHA 18001, ISO 14001, HACCP..............

    Hazard Communication Training for meeting DOT, OSHA, OSHA 18001, ISO 14001, HACCP..

    OHSAS 18001: Executive & Management Overview

    OHSAS 18001: Internal Auditing/Auditor and Implementation

    ISO 20000 (Information technology: Service management): Internal Auditing/Auditor and Implementation

    ISO 22000 Food safety management systems: Internal Auditor/Auditing training and implementation

    ISO 27001 Information Security Management: Internal Auditing Training and Implementation

    Training by Industry:
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    Bank of America | FedEx | Hitachi  Johnson and Johnson | JP Morgan Chase  NVIDIA | USDA | Roche | ARIVA  Kellogg | Sears

    City of Dallas | Michigan State University | GE Healthcare | Cesna Aircraft | Magnolia Beef Company  Central Coast Seafood

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