Pathologists and study directors in nonclinical research are under increasing pressure to deliver high-quality results faster, without compromising data integrity. Traditional, manual methods of data entry are too slow, error-prone and unstructured to meet the demands of today’s fast-paced, high-throughput labs. That’s why modern pathology teams are turning to efficient, standardized digital tools to accelerate workflows, reduce human error and improve overall productivity in conducting non-GLP pathology studies.

Another goal of an optimized pathology workflow is transforming how studies are managed, recorded and scaled for future success. With smarter digital systems, labs can gain immediate efficiency while laying the groundwork for regulatory readiness down the road.

In this webinar, the featured speakers will explore how pathology teams can modernize their approach to study management with tools designed specifically for fast, intuitive, and reliable histopathology workflows. For teams aiming to optimize current non-GLP processes or prepare for future GLP compliance, this session will offer practical insights to support confident progress.

Join the pathology experts as they demonstrate how digital tools and workflows can:

Reduce slide review and data entry time by up to 20% using streamlined digital workflows built for non-GLP environments
Improve data integrity and accessibility with structured study management tools offering a single source of truth for moderated access and editing
Streamline glossary management with integrated terminology support based on CDISC ontology and intelligent search features
Manage non-GLP studies more efficiently through flexible, user-friendly platforms that support better team coordination and faster study completion
Prepare labs for future GLP compliance by adopting digital tools that align with industry standards and regulatory expectations

Register for this webinar to learn how digital transformation can drive efficiency and readiness across pathology studies, supporting pathologists, study directors, lab managers and more.

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Speakers

Chris Nichols, Senior Director, Instem

Chris Nichols is a leading expert and educator in the scientific community, specializing in the successful application of study management solutions. Intimately familiar with research workflows in discovery, genetox, pathology and everything in between, Chris brings a wealth of knowledge and experience when it comes to optimizing lab practices and leveraging digital solutions that improve research outcomes.

Message Presenter

Chris Hunter, Product Manager, Pathology Study Management, Instem

Chris Hunter is a Product Manager focused on driving innovation in healthcare tech. He has a passion for transforming complex challenges into seamless, user-centric solutions. Chris specializes in agile product management within the pathology and healthcare SaaS industry, and he thrives at the intersection of technology, user experience and business strategy, delivering data-driven innovations that enhance efficiency and optimize workflows.

Message Presenter

Who Should Attend?

This webinar is designed for professionals in pharmaceutical, biotech and contract research organization (CRO) organizations, including:

Lab Managers and Directors looking to improve lab efficiency, compliance and data integrity
Principal Investigators and Scientists seeking better ways to capture, organize and manage experimental data
Pathologists and pathology experts

What You Will Learn

Attendees will:

Learn how streamlined workflows and intuitive interfaces help pathologists reduce time spent on slide review and data capture — freeing up hours for deeper analysis
See how built-in checks, standardized terminology and smart glossaries reduce errors and ensure pathology data can be trusted throughout the study lifecycle
Discover how efficient, flexible tools can support non-GLP pathology studies without sacrificing structure — helping study directors manage timelines, staff and results more effectively

Xtalks Partner

Instem

A global provider of leading software solutions and scientific services, Instem is helping our customers discover, accelerate, and advance key R&D programs by offering solutions powered by science and best practices in research.

We enable organizations in the life sciences to more efficiently collect, report and submit high quality regulatory data, while offering them the unique ability to generate new knowledge through the extraction and harmonization of actionable scientific information.

Across the entire drug development value chain, every day Instem solutions are meeting the rapidly expanding needs of life science organizations for data-driven decision making, leading to safer, more effective products. Founded in the United Kingdom in 1969, Instem has deep roots internationally across North America, EMEA and APAC. We maintain a commercial and technical presence throughout these regions and pride ourselves on localized support for our diverse client base.