Regulatory training that doesn’t make you want to poke your eyes out

Let’s be honest: most compliance training is either a) a snoozefest, b) a 400 page PDF you’ll never read, or c) a patronising PowerPoint that tells you to "consult your regulatory team" without ever explaining what that actually means.

We built Taylored Training to be none of those things.

When you work in cosmetics, supplements, or medical devices, you can’t afford to not understand the regs. But you also don’t have time to become a full time compliance expert. That’s where we come in.

Our training sessions are practical, digestible, and actually enjoyable (yes, really). They’re built for busy teams who want to get confident with the basics and finally understand what those endless acronyms and grey areas actually mean in real life.

Here’s what’s on offer:

Medical Devices Overview

This one’s for anyone who’s ever asked: Is this actually a medical device We walk you through what makes a product a medical device (and what doesn’t), explain what the classification rules mean, and help you understand what you’re actually signing up for when you put CE or UKCA on a label. Whether you're launching your first device or onboarding new team members, this is a fast track to feeling less confused and more in control.

How will you benefit? This course will help you understand the key requirements and concepts of Regulation (EU) 2017 745 and the UK Medical Devices Regulations 2002, and how to apply that knowledge to real products in your business.

What you’ll learn:

• Overview of both EU MDR and UK MDR
• Key compliance responsibilities across functions like R&D, supply chain, marketing, and QA
• How to define and classify your product
• What the different device classes actually mean
• How to put together a proper technical file
• The basics of CE and UKCA marking
• What a notified body does, and when you need one
• How to register your device in the UK and EU
• What’s required in your Quality Management System
• Intro to post market surveillance
• And of course, how Brexit fits into all of this

Who should attend?

• New starters in Regulatory Affairs
• People expanding their RA responsibilities to include medical devices
• Anyone working with RA teams who needs to know the lingo Note: This training does not cover In Vitro Diagnostics (IVDs)

What's included? It’s an in-person session, with proper content materials sent out after the course so you’re not frantically scribbling notes the whole time.

Why we built this

Because we were sick of seeing people get caught out by confusing rules that no one ever explains properly.

Because our clients were constantly saying “we didn’t know we needed that”.

Because Googling regulatory advice at midnight is not a viable compliance strategy.

If you’re ready to stop second guessing everything and start understanding what you actually need to do without falling asleep in the process, check out our training sessions at Taylored Consultancy.

We promise no death by PowerPoint. Just proper, practical help. Book your place for our October workshop here:

Oct 15, 2025 9:00 AM

Taylored Consultancy Ltd, 3 Wharfside Street, Spaces The Mailbox Level 1, Birmingham, B1 1RD

https://www.tayloredconsultancy.co.uk/product/medical-device-training-mdr

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