Category: Webinar

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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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Understand the Applicability of FDA’s Computer Software Assurance Guidance to Data Integrity

“Computer System Validation” (CSV) has remained mostly unchanged for the past two decades. General Principles of Software Validation (GPSV), issued by the FDA in 2002, has been and continues to be the primary tool industry uses as guidance on this topic. CSV, as it stands today, is a documentation heavy exercise Documentation is done at […]

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Operational Excellence: Does Your Site Truly Take Continuous Improvement Seriously?

The earliest documented interest in Operational Excellence (OPEX) in the pharmaceutical industry occurred in the late 1990s – twenty years after other manufacturing sectors began to think of OPEX as a competitive imperative. Since then, little progress has been made based on our experience working with clients. In some cases, tremendous short-term improvements are made […]

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Risk-Based EM Sampling Strategy – Using the Process Risk Control Strategy to Determine EM Sampling Strategy

Join us as we discuss four different ways of using the process risk control strategy to determine EM sampling.Part 1 – Holistic Process Risk Control Strategy• Process Risk Assessment and establishing a holistic riskcontrol strategy• Environmental risks and risk controlsPart 2 – Environmental CQAs and CPPs• Environmental CPPs and the product CQAs impacted• ISO classifications […]

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