On-Demand Webinars
-
Effective And Flexible Packaging, Labeling And Distribution Strategies For Diverse Drug Types
3/24/2026
Learn how demand-led and hybrid clinical supply models reduce waste, accelerate timelines, and improve flexibility for global trials through regional hubs and patient-specific packaging strategies.
-
Improving Supply Chain: Accountability, Sustainability, Optimization
Watch as industry experts explore the advancements in drug accountability facilitated through IRT, encompassing innovative methods for managing site variations and sustainable supply chains.
-
Agile IRT/RTSM - Enabling Clinical Trial Design And Supply Innovation
1/20/2022
This webinar demystifies the term “agile,” from an operational perspective, while highlighting the speed and flexibility these systems offer to be able to support complex protocols that require accelerated changes.
-
Client Sustainability Directives — CDMO Perspectives
9/16/2024
Gain a deeper understanding of current directives and metrics to equip your team with the knowledge necessary to navigate the evolving landscape of sustainability.
-
Minimize Sample Loss With Proactive Logistical Planning And Technologies
3/8/2022
The complexities of sample collection and logistics in advanced therapy studies naturally brings chain of custody challenges in protecting the integrity of a trials’ high value samples. Learn about end to end sample management strategies, logistical integration planning, real-time tracking and LIVE monitoring technologies.
-
The Future Of Drug Storage And Distribution
8/22/2023
Consider these strategies when anticipating and mitigating disruptions, and how future innovations and trends will continue to shape the logistics industry.
-
Essential Up-Front Planning For Your Clinical Trial
Early planning mitigates risk by avoiding stock outs and study delays, minimizing waste with optimized inventory, and forecasting demand to facilitate robust supply planning.
-
Mitigating Risk And Complexity In Cell & Gene Therapy Trials With IRT
8/19/2025
CGT pioneers require supply chain partnerships that mitigate trial risk and complexity. Explore how to optimize pre-trial and pre-screening activities and reduce trial cost and risk with an IRT solution.
-
Smart Packaging In Clinical Trials: The Power Of Adherence Data
Individual data points over time can provide precise drug dosing histories that enable better understanding of protocol adherence, safety, efficacy, PK/PD and a drug’s exposure-response relationship.
-
Navigating Complex Supply Chains: The Critical Role Of UK And EU Qualified Persons
3/4/2026
Gain essential insights into QP roles, regulatory updates, and best practices for ensuring compliance, supply continuity, and safe handling of cold and frozen pharmaceutical products across the UK and EU.