Blog

Comply Guru is excited to announce a new strategic partnership with Clinius Oy in Finland, a pioneer in clinical device trials who are a device CRO specializing in clinical device studies, product documentation and quality systems for the Medical Device Industry.

Today I am proud to announce our new & improved website for Ireland, UK and the U.S is now live! I have personally managed this project as I sought to make various improvements across the entire website.

While the EU Medical Device Regulation (MDR) brings numerous improvements, it also poses several challenges that need to be addressed. In this blog, I discuss five of the challenges under the European Medical Device Regulation.

One of the most common questions I am asked relates to whether internal auditor or lead auditor training is the right choice. The answer is it depends on several factors. Let’s discuss.

Let’s talk about Blended Learning. In 2019, Comply Guru set out to create a new approach to conventional Auditor Training, launching it’s first CQI & IRCA Accredited Blended ISO 9001 Internal Auditor Training Course (No. 2149) in March of the same year.