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Kenneth Gutiérrez

Director, Product

Kenneth Gutiérrez is the Director of Product at Docuvera, where he leads product strategy for a platform that helps pharmaceutical companies author, govern, and reuse regulated content. Kenneth describes his approach as “science background, business foreground” — a perspective built on rational drug design and pre-clinical academic research in biochemistry at Texas Tech University and a STEM MBA from the Rawls College of Business, and refined through 15+ years of life sciences experience spanning early-stage drug research and enterprise SaaS product management, including more than five years at Agilent Technologies leading customer success onboarding and global pricing strategy for life sciences software. 

At Docuvera, Kenneth leads the full product organization — including product managers and product owners across agile delivery — overseeing platform direction, web experience, and integrations.

Kenneth Gutiérrez, Director of Product at Docuvera

Kenneth’s product focus is squarely on the challenges that matter most to regulated teams: governance-first structured content authoring, ePI readiness, IDMP-aligned content strategy, health authority interactions, and interoperable content workflows. He is a regular contributor to industry conversations on these topics, presenting alongside the Docuvera team at DIA webinars and forums — where his dual fluency in scientific practice and product strategy grounds technical discussions in real operational requirements. 

Read Docuvera’s AI and structured content readiness framework at https://docuvera.com/blog/how-to-assess-ai-and-structured-content-readiness/ or connect with Kenneth on LinkedIn https://www.linkedin.com/in/kenneth-glenn-galloway/

Posts by Kenneth Gutiérrez

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SmPC to ePI: Navigating ePI Implementation

How pharma teams can prepare for structured product information, FHIR readiness, and EU ePI standard…

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ePI and FHIR: A Practitioner’s Walkthrough of the FHIR ePI Implementation Guide

What Pharma Companies Need to Know About ePI FHIR When the European medicines regulatory network a…

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ePI vs SPL: Preparing for EU Electronic Product Information and FDA Structured Product Labeling

How EU ePI and FDA SPL Create Parallel Labeling Workflows A director of Regulatory Affairs at a mi…

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Scaling Globally Without Slowing Down: Why Global Pharma Growth Depends on Global Labeling Harmonization

Global growth in pharma increases complexity before it increases value. This article explains why gl…

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