Training

Practical training for management-system professionals

Build standards knowledge and practical internal-audit skills through focused online courses from TQS Services.

One straightforward path

How it works

  1. Choose your courseCompare the available standards and select the training that fits your work.
  2. Create your accountCheck out securely so your progress and certificate stay with your individual account.
  3. Learn at your paceComplete the lessons, practical guidance, and final assessment online.
  4. Download your certificateAfter completing the course requirements, access your certificate from My Account.

Typical completion timePlan for approximately 6–10 hours, depending on the course and your pace. You can stop and return as your schedule allows.

Lifetime course accessYour purchased course access does not expire. Return to the lessons and your certificate from My Account whenever you need them.

Prefer to speak with a person?Visit our Contact page and fill out the short form. A TQS Services team member will respond within 24–48 business hours to help you choose training or arrange your purchase.

Contact TQS

Available training

$299.99

NIST SP 800-171 Revision 3 Implementation and Internal Assessment

Training for your whole team

Buying training for multiple people?

Purchase every seat in one checkout, then invite participants when you are ready. Each learner receives a private account, individual progress, and their own certificate while the buyer keeps control of orders and billing.

  • Choose courses and seat quantities together
  • Assign names and email addresses from My Account
  • Let every participant begin as soon as their seat is assigned
Simple purchasing. Private learner access.Explore Team Training

Current transition guidance

Move from the legacy FDA QSR to the effective QMSR.

Use a professional implementation playbook built around the FDA QMSR effective February 2, 2026, ISO 13485:2016, and the supplemental FDA requirements that medical-device organizations still need to control.

FDA QMSR transition guide from legacy 21 CFR Part 820 to ISO 13485:2016

FDA QMSR + ISO 13485:2016

FDA QMSR Transition Guide: Legacy 21 CFR Part 820 to ISO 13485:2016

Move a legacy FDA Quality System Regulation program into the effective 2026 QMSR with a practical gap assessment, 12-week roadmap, evidence checklists, and implementation worksheets.

  • 31-page current 2026 edition
  • Gap assessment and 12-week roadmap
  • Inspection evidence and action worksheets

This original TQS guide summarizes implementation considerations. It does not include or replace a licensed copy of ISO 13485:2016 or provide legal advice.

From learning to fieldwork

Take an organized audit system with you.

Each field kit turns the course concepts into an editable working system for planning, collecting objective evidence, writing findings, tracking corrective action, and reporting results.

ISO 9001:2015 editable audit toolkit

ISO 9001:2015

ISO 9001:2015 Internal Audit Field Kit

Plan, conduct, document, report, and follow up a quality-management-system internal audit in one editable workbook.

  • Editable Excel workbook
  • Audit workflow and user guide
  • Instant protected download
AS9100 Rev. D editable audit toolkit

AS9100 Rev. D

AS9100 Rev. D Internal Audit Field Kit

Carry aerospace audit planning, objective evidence, sampling, findings, corrective action, and reporting in one editable workbook.

  • Editable Excel workbook
  • Audit workflow and user guide
  • Instant protected download
ISO 13485:2016 editable audit toolkit

ISO 13485:2016

ISO 13485:2016 Internal Audit Field Kit

Organize medical-device QMS audit planning, regulatory-aware prompts, evidence, findings, CAPA follow-up, and reporting.

  • Editable Excel workbook
  • Audit workflow and user guide
  • Instant protected download
ISO/IEC 27001:2022 editable audit toolkit

ISO/IEC 27001:2022

ISO/IEC 27001:2022 Internal Audit Field Kit

Connect ISMS risks, the Statement of Applicability, evidence, sampling, findings, corrective action, and management reporting.

  • Editable Excel workbook
  • Audit workflow and user guide
  • Instant protected download
ISO 14001:2015 editable audit toolkit

ISO 14001:2015

ISO 14001:2015 Internal Audit Field Kit

Organize environmental aspects, compliance obligations, lifecycle controls, evidence, sampling, findings, corrective action, and reporting.

  • Editable Excel workbook
  • Audit workflow and user guide
  • Instant protected download
ISO 45001:2018 editable audit toolkit

ISO 45001:2018

ISO 45001:2018 Internal Audit Field Kit

Organize hazards, worker participation, legal obligations, operational controls, evidence, incidents, corrective action, and reporting.

  • Editable Excel workbook
  • Audit workflow and user guide
  • Instant protected download

Field kits are original TQS working tools. They do not include or replace a licensed copy of any standard.