Upcoming Live Webinars
| Title | Date | Start Time | Duration | Register |
|---|---|---|---|---|
| Clean by Design: Navigating Medical Device Cleanliness Through Validation, Regulatory Alignment, and Failure Response
In medical device manufacturing, “clean” is not a one-time achievement; it’s an ongoing process that must remain controlled, defensible, and aligned with patient safety. Yet even well-designed cleaning strategies can be challenged by real-world conditions, evolving regulatory expectations, and unexpected results. This webinar explores three common scenarios manufacturers face and provides a practical framework for cleaning validation interpreting outcomes and determining next steps: • Initial Cleaning Validation (and Revalidation Triggers) Defining “clean,” selecting appropriate methods, and building a robust validation approach are critical, not only for initial success, but for managing future changes with confidence. • Regulatory Scrutiny and Notified Body Challenges Increasing expectations from notified bodies and regulators can expose gaps in cleaning rationale, acceptance criteria, or validation strategy, often late in the process. • Excursions in Established Processes When validated cleaning processes drift, due to variability, contamination events, or manufacturing changes, teams must determine impact, root cause, and whether revalidation is required. Through real-world examples, we’ll walk through how to evaluate each scenario, connect cleaning data to risk, and take appropriate, defensible action. Attendees will learn how to: • Define and justify “clean” using risk-based approaches • Interpret cleaning results in context, not in isolation • Strengthen validation strategies to withstand regulatory scrutiny • Assess the impact of excursions and process changes • Make informed decisions that support both compliance and patient safety | 7/22/2026 | 2:00pm EDT | 1 hour | Register |
| Go with the Flow: Strengths, Limitations, and Real-World Applications of Rheological Testing
In this webinar, Cambridge Polymer Group experts go beyond theory to explore when and how rheology delivers meaningful insight, where it falls short, and how to interpret results in the context of real materials, real processes, and real failures. Through practical examples and case studies, we will examine how rheological measurements are applied to polymers, elastomers, and formulated systems—and how improper test selection or interpretation can lead to incorrect conclusions. Attendees will gain a clearer understanding of rheology’s strengths and limitations and learn how to use it more effectively in R&D, manufacturing, troubleshooting, and product qualification. This webinar is ideal for technical professionals who want to improve decision-making, reduce development risk, and better connect rheology data to performance and process outcomes. | 8/19/2026 | 2:00pm EDT | 1 hour | Register |
Past Webinar Recordings
Recording name Created Date Download Beads, Barriers, and Cleaners: How Material Science Safeguards Consumer Products 4/15/2026 Download Age ISN’T Just A Number: Accelerated Aging Methods for Material and Product Characterization 1/21/2026 Download Getting Material Selection Right the First Time 11/12/2025 Download From Residues to Risk: The Role of Cleaning Validation in Biocompatibility Assessments 10/15/2025 Download Material Deformulation: Because Ignorance Is NOT Bliss (Especially When Your Product Fails) 9/17/2025 Download Squeezing the Most Out of Medical Device Hydrogels 8/13/2025 Download The Tightrope of Tentative IDs: Balancing Analytical Uncertainty with Toxicological Risk Assessment 7/9/2025 Download
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