Category: Lab

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Stability Considerations for Drug-Device Combination Products-21 CFR Part 4 Update

Created by: Chris Latoz & Kim Huynh-baCombination products are therapeutic and diagnostic products that include two or more of the following: drug, biologic, and device. These products are needed for enhanced clinical outcomes and have more than one Mode of Action (MOA). Therefore, they require a more complex regulatory pathway and compliance with a minimum […]

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Medical Product Excursions from Labeled Storage Conditions

Created by: John O’Neill, Facilitator, PSDG, Editor, StabilityHub.comStability excursions are unintended lapses in the control parameters (such as temperature, relative humidity, and light) which are designed to preserve a product at experimental, manufacturing, shipping, and patient environment conditions. Significant excursions bring into doubt the validity of data generated in stability studies and the integrity of […]

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Developing a Laboratory Disaster Plan

Created by: Christopher V. Latoz, Stability Manager, Hollister Incorporated Many laboratories have not taken the time to develop a disaster plan, or the plan they have created has not been reviewed or revised for several years. In this article, we’ll discuss key elements that should be incorporated in a laboratory disaster plan, including a hazard […]

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Unleashing the Power of AI: Practical Applications in Computer System Compliance

What are the main benefits of standardization of validation processes, and how do you drive standardization across an organization How do you benchmark how mature your validation processes are, and what standards to drive for. Create comprehensive training packages to align validation practices globally Focus on creating a risk-based culture How investment in technology can […]

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