We’d like to introduce you to Bob Rogers, who joined our regulatory team in November.

He is a senior quality assurance and regulatory affairs professional with over 20 years of experience working with medical device regulations in the US, EU, Canada, and Australia.

He’s co-located in Boston and the DC area, working with our US clients as well as those in Europe.

He has been responsible for building full regulatory teams, including the QA/RA Manager and Management Representative. Also, formed and led a worldwide multi-disciplinary team to ensure compliance with Unique Device Identification requirements.

Beyond his work as a regulatory advisor, he’s also serves as an expert witness for litigation in the US.

On behalf of our growing team, welcome to Digital Health Works.