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Strategic Impact of Vendor Management and Oversight
Read more »: Strategic Impact of Vendor Management and OversightPart 2: Resource Optimisation Welcome back to our series on the strategic impact of vendor management and oversight in clinical trials. In part one, we discussed the importance of risk management. In this article, we explore how resource optimisation in vendor management and oversight impacts: Below is a list of some common methods that businesses…
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Aligning Vendor Management with Strategic goals for Clinical Trial Sponsors
Read more »: Aligning Vendor Management with Strategic goals for Clinical Trial SponsorsPart 1 – Risk Management Clinical trial sponsors face numerous challenges in managing vendors and ensuring the success of their trials. Clinical trial sponsors must take a strategic approach to vendor management. This involves aligning vendor management with business strategy to ensure that vendors are selected, managed, and evaluated in a way that supports the…
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Key Processes in Vendor Management and Oversight: A Deep Dive into Effective QMS
Read more »: Key Processes in Vendor Management and Oversight: A Deep Dive into Effective QMSEffective vendor management and oversight are critical to the success of a clinical trial. It’s not just about choosing the right vendors but also about efficiently managing and overseeing them throughout the trial. By integrating these key processes into your QMS, you’re creating a comprehensive system that aids in reducing risks, improving quality, and facilitating…
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Best Practices for Maintaining Regulatory Compliance in Vendor Management and Oversight
Read more »: Best Practices for Maintaining Regulatory Compliance in Vendor Management and OversightClinical Trials are complex and even more so when multiple key deliverables are outsourced by Sponsors. It is critical for Sponsors to ensure regulatory compliance and patient safety and data integrity. The cost of non-compliance can be significant and anxiety-inducing to the most diligent clinical research professionals. Regulatory inspection findings can lead to increased scrutiny,…
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Applying Principles of FDA Guidance for Industry Q9 Quality Risk Management 2023 to Vendor Risk Management
Read more »: Applying Principles of FDA Guidance for Industry Q9 Quality Risk Management 2023 to Vendor Risk ManagementThe FDA guidance on quality risk management released in May (2023) offers principles and examples applicable to various pharmaceutical quality aspects. The principles of quality risk management in this guidance can be extended to clinical trial vendor risk management, covering different stages of a clinical trial. When applied to clinical trial vendor risk management, the…
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Vendor Level vs Study Level Vendor Risk Assessment: A Robust Approach
Read more »: Vendor Level vs Study Level Vendor Risk Assessment: A Robust ApproachClinical trial vendor management requires a strategic approach, proactive thinking, and a deep understanding of vendor risk assessment at both the vendor and study levels. Two approaches to vendor risk assessment — vendor level and study level — serve to manage different types of risk. The assessments are complementary and critical to clinical trial delivery.…
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Welcome to Mayet: Spearheading change in Clinical Research Vendor Management
Read more »: Welcome to Mayet: Spearheading change in Clinical Research Vendor ManagementWe are excited to introduce Mayet, an innovative all-in-one solution in the world of clinical research outsourcing. Clinical research is a vital process that opens new avenues for treatment. However, it is fraught with complexities and challenges, particularly in the realm of vendor management. Fragmented systems, inefficient processes, lack of visibility, and increased risk are…