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Optimizing Ancillary Sourcing in Clinical Trials: Expert Insights from Myonex

From kits and equipment to global regulations, ancillary sourcing plays a critical role in the success of your clinical trial. Yet, many sponsors still underestimate the risks, inefficiencies, and added costs that come with fragmented or ad-hoc approaches.

In this video series, we sat down with Marla Dilday, Associate Director of Ancillary Sourcing at Myonex, to explore three challenges sponsors commonly face, and how to solve them.

What should you know about…

Discover practical strategies to streamline operations, ensure compliance, and gain flexibility across your ancillary supply chain. Whether you’re designing kits, leasing equipment, or navigating import/export hurdles, this series offers expert guidance rooted in real-world experience.

What should you know about Ancillary Kitting or Convenience Kitting in Clinical Trials?

Ancillary supplies that aren’t optimized into kits often lead to excess inventory, wasted resources, and unnecessary complexity for sites and patients.

In this video, Marla Dilday explains how tailored kitting – whether lab, infusion, or patient kits – can improve efficiency, enhance consistency, and support better outcomes.

The result? Reduced waste, improved protocol adherence, and cost-effective operations across global trials.

Watch the video to see how Myonex brings structure and simplicity to ancillary kitting.

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What should you know about Equipment Leasing in Clinical Trials?

With rising budget pressure, sponsors are increasingly turning to equipment leasing to manage trial costs.

In this video, Marla breaks down how short and long-term leasing options from Myonex help sponsors stay agile, without sacrificing compliance or performance.

From global coverage to ongoing calibration and maintenance, Myonex supports your equipment needs across the entire lifecycle of the study.

Watch the video to explore how leasing can bring flexibility and budget control to your trial operations.

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What should you know about Import/Export Regulations for Medical Devices (MD) in Clinical Trials?

Navigating international regulations is one of the most underestimated, and potentially costly, challenges in MD sourcing.

In this video, Marla outlines how Myonex helps sponsors manage documentation, customs clearance, and compliance with evolving global standards.

With expert support from our medical device sourcing teams, you can avoid delays, prevent compliance risks, and keep your trial on track.

Watch the video to learn how Myonex simplifies and secures your medical device import/export.

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Ready to turn ancillary sourcing from a stress factor into a smooth, reliable process?

From custom kitting and equipment leasing to medical device import/export, Myonex provides expert-driven solutions designed to reduce risk, improve efficiency, and support trial success.

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