What does Datod Consulting do?



Datod Consulting helps medical device companies transform their Quality Management Systems (QMS) to be faster, leaner, and fully compliant. We work with ISO 13485, FDA 21 CFR Part 820, and other regulatory frameworks, providing hands-on solutions that improve quality outcomes and reduce business risk.

Who do you work with?

We partner with medical device manufacturers, in vitro diagnostics companies, and related healthcare technology firms—whether they’re start-ups preparing for market entry or established businesses seeking process improvement.

What results can you deliver?

Our clients typically see measurable improvements within months.
For example:

• Reduced CAPA process steps by 70%
• Reduced approval bottlenecks by 85%
• Cut product recalls by 50% in some cases

How is Datod different from other consultancies?

We combine deep regulatory knowledge with practical, real-world solutions. Many consultants tell you what’s wrong—we show you exactly how to fix it, and we stay engaged until results are embedded.

We also offer free structured training to upskill your team.

Do you only work in the UK?



No. While we are based in Wales, we work with companies across the UK, Europe, and internationally through virtual and hybrid consulting models.

What’s included in your free training?

Our free 12-hour course covers:

• Building a quality mindset
• Risk management
• Change control
• Continuous improvement
• CAPA effectiveness
  

It’s designed for practical application, not theory. In addition there's a free QMS assessment to give you in-depth analysis and help.

Do you work on short-term projects or ongoing support?

Both. We can provide rapid interventions for urgent compliance issues or long-term partnerships to steadily improve your QMS performance.

How can I get started?

Simply contact us to arrange an initial conversation. We’ll assess your needs, outline potential improvements, and recommend a tailored plan—no obligation.