Derek Lord

Derek Lord

With over 10 years in the technology industry, Derek Lord applies his problem-solving skills and logical mind to help clients achieve their organizational and workflow goals. In his role on the Professional Services team at DistillerSR, Derek has been directly involved in implementing medical device clinical evaluation report solutions and best practices for clients producing reports for device approval in the EU. He has consistently achieved a five-star rating for his work developing project templates for medical device literature review.
What is Regulatory-Grade AI?

What is Regulatory-Grade AI?

We keep getting asked the same question: if we use general-purpose AI tools to support a regulatory submission, will the output stand up to a regulator, a payer, or a notified body? Every day, medical affairs, HEOR, and regulatory teams conduct literature reviews that...