Resources
Explore our Resource Hub: On-Demand Webinars, Brochures, Case Studies, and Insights to Accelerate Your Research.
Resource Type
On-Demand Webinar: When SEND Quality Matters Most
This webinar shows how Instem’s SEND Advantage™ Services help sponsors and CROs reduce submission risk, meet the FDA’s evolving expectations for dataset quality, and submit with confidence through expert-led SEND conversion, verification, and regulatory consultation.
On-Demand Webinar: Closing Compliance Gaps with Compliance Builder
This webinar shows how Compliance Builder enables regulated laboratories to close audit gaps, strengthen data integrity, and meet 21 CFR Part 11 requirements through real-time monitoring, automated audit trails, and layered security controls designed for...
On-Demand Webinar: Advanced Colony Management with Climb
This webinar shows how Climb enables research teams to streamline colony operations through structured animal tracking, real time health monitoring, and integrated scheduling tools designed to improve accuracy, efficiency, and compliance across modern in vivo...
How to Safely Harness R and SAS for Cutting-Edge and Validated Clinical Analytics
Watch our on-demand webinar to discover how to best leverage R and SAS for a multilanguage approach to biostatistics, while staying compliant.
On-Demand Webinar: Accelerating Data Entry for Non-GLP Pathology Studies with Provantis
This on-demand webinar shows how Provantis enables pathology teams to accelerate non-GLP study workflows by optimizing pathology data capture, improving data integrity, and preparing labs for future regulatory readiness.
On Demand Webinar: Beyond Data Management: The Strategic Benefits of Modern LIMS?
Discover how modern LIMS empowers laboratories to streamline workflows, strengthen compliance, and transform data into meaningful insight.
On-Demand Webinar: Modernizing Non-GLP Study Management with Climb
Discover how Climb is transforming Non-GLP study management for preclinical research teams.
Preclinical Drug Discovery: Turning Drug Safety Data into Decisions
Exploring the key technological capabilities driving innovation in drug safety and regulatory science.
Does SEND pave the way for creating Virtual Control Groups?
This session will discuss the opportunities for data use beyond submissions, specifically in the area of constructing virtual control groups.
Empower Your Research
Start Your Transformation Today
