|
|
|
|
|
|
|
|
|
Webinar: Design Verification Done Right: Smarter Strategies for Prefillable Syringes
|
Design verification for prefillable syringes can be challenging as regulatory expectations, drug-device integration, and testing requirements evolve. This webinar explores a risk-based framework for building a defensible verification strategy. Using a real-world case study, learn how to translate user requirements and product targets into test plans, acceptance criteria, and aging considerations. Gain insights to strengthen decisions and reduce ambiguity. Click here to learn more.
|
|
|
|
|
|
Webinar | PTI Packaging and Inspection Systems
|
Gain practical insights into the future of package validation, including smarter aging studies, science-based decision-making, and how validation professionals can move beyond legacy practices.
|
|
|
|
|
|
Webinar | Particle Measuring Systems
|
Discover how modern strategies like the CCS are transforming environmental monitoring by exposing hidden risks, enhancing data quality, and unlocking deeper insights through innovative methods.
|
|
|
|
|
|
Video | Adare Pharma Solutions
|
See how innovative technologies, global reach, and commitment to quality and patient-centricity can deliver exceptional solutions for your oral solid dose needs.
|
|
|
|
|
|
Video | West Pharmaceutical Services, Inc.
|
As a trusted partner to both established and emerging drug developers, we support the safe, effective containment and delivery of life-saving and life-enhancing medicines.
|
|
|
|
|
|
Video | Pharmaceutical Online
|
In this segment from the Pharmaceutical Online Live event, our panelists talk about quantifying and characterizing your impurities. They discuss two levels of LC-MS in the future for better impurity profiling.
|
|
|
|
|
|
Video | Anritsu - Product Inspection & Detection
|
Protect your production yield and eliminate costly line disruptions. Watch this data-driven analysis to explore how specialized inspection limits drastically lower false reject rates.
|
|
|
|
|
|
|
|
|
|
Building a Science- and Risk-Based Bio-decontamination Strategy
|
This webinar explores how bio-decontamination has become a critical component of sterility assurance under evolving regulatory expectations, including EU GMP Annex 1. Attendees will learn a lifecycle-based approach to contamination control, covering microbial inactivation science, decontamination technology selection, cycle development, validation (IQ/OQ/PQ), and routine monitoring. The session provides practical guidance for building and maintaining a compliant, defensible biodecontamination strategy for isolators and barrier systems.
|
|
|
| Connect With Pharmaceutical Online: |
|
|
|
|
