Pascal Werner Daniel Young 25 August 2023

Hello, I'm Pascal...

"In the last years I enjoyed working on the intersection of business, engineering, and legal (data privacy/GDPR and medical device certification)."
He's not only a SaMD expert, but he also has a engineering background and knows his way around coding.

Pascal Werner is a quality management and regulatory affairs consultant with over seven years of experience in the EU with a strong focus on software as a medical device, especially AI and digital therapeutics.

He holds a master degree in biomedical engineering, has cofounded a startup previously, and has hands-on experience in software development.

Pascal has a proven history of setting up or building out quality and information security management systems as well as crafting and reviewing technical documentations, including clinical evaluation, software file, usability engineering, risk management. Relevant norms include ISO 13485, IEC 62304, ISO 14971, and IEC 81001-5-1 amongst others. This work also includes performance of internal audits as well as management of internal audits.

He prefers working with clients to build out a good quality culture and strong processes where passing audits and reviews becomes second nature. However, he has also experience in remediating findings in technical documentation reviews as well as audit non-conformities.

Contact Digital Health Works

Pascal is an experienced advisor on regulations for companies developing SaMD products. 

When you have questions on where to get started, and how to move your regulatory work forward, let’s find a time to speak.

Let's start a conversation...

[contact-form-7 id="77808"]