Template: List of Training Documentation

Sven Piechottka • ISO 13485 Templates • Published June 09, 2022 • Human Resources

Template Download

This is a free template, provided by OpenRegulatory.
If you are a user of Formwork, our eQMS software, you can save a lot of time by choosing “QMS” on the top menu and “OpenRegulatory Templates” on the left menu, then opening the relevant folder to find this template ready to load into Formwork.

If, for some mysterious reason, you're using a different QMS software, you can also simply download this template – specifically, as Word (.docx), PDF, Google Docs or Markdown file. Scroll down for a preview!

The template license applies (don't remove the copyright at the bottom, don't re-use this for commercial purposes).

Download Word File DOCX

Download PDF PDF

Download HTML (Google Docs) HTML

Download Markdown MD

Lost In Regulation? We're here to help.

Unsure how to get started and how to get your EU MDR medical device certified?
We've already helped 100+ companies with their MDR compliance.
Take a look at our services and book a free 30-minute consulting call.

Chat with us now → View Services & Pricing →

Document Template

Template Preview

List of Training Documentation

This template is supposed to give you an idea of the structure. Don't use Microsoft Word - this is thought
as an Excel / sheets file.

Also, think of this as two tabs - one for initial and one for continuous training.

Initial Training

Employee	Start of Employment	Job Role	Training #1: QMS Intro	Date Due	Date Completed	Effectiveness	Training #2: Data Privacy	(...)
Jack Rack	01.04.2021	Sales Manager	Applicable	15.04.2021	14.04.2021	Confirmed by supervisor	Applicable

Continuous Training

Name of Training	Type of Training	Due Date	Participant #1	Date Completed	Effectiveness Check	Participant #2	Date Completed
Annual Data Privacy Training	Recurring	01.04.2021	Applicable	14.04.2021	Confirmed by questionnaire	Applicable	14.04.2021
Code of Conduct	New SOP	01.05.2021	Applicable	03.05.2021	Confirmed by questionnaire	Applicable	03.05.2021
Development Process	Updated SOP	01.05.2021	N/A			Applicable	03.05.2021

Template Copyright openregulatory.com. See template
license.

Please don't remove this notice even if you've modified contents of this template.

Sven Piechottka

With a background in political and administrative sciences, my way into regulatory affairs started from a different angle. I focused on the promises of precision medicine during my final year of studies and first joined IBM to help leverage healthcare innovation projects across Germany.

I then gained most of my regulatory experience while working for Vara (before: Merantix Healthcare), where we built up a quality management system from scratch. For about three years, I coordinated regulatory affairs, led the ISO 13485 certification and CE certification of an AI-based radiology software, and served as data protection officer and quality management officer of the company.

More about me