Article
Navigating Common Clinical Supply Challenges For Asia-Pacific Regional Studies
Summary: Unlike well-established clinical trial regions, such as Europe which benefit from more harmonized regulatory requirements and quality standards and transportation networks, the APAC region is a collection of independent countries each with its own infrastructure limitations, clinical supply quality standards, regulations, and protocols...
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Webinars
Leveraging Forecasting Models To Optimize Clinical Trial Supply Management
Summary: Explore how to drive excellence within the forecasting process and how to utilize forecasting throughout the study to plan for study clinical supply budgets and identify potential supply-related issues before they negatively impact your study...
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Article
The Medicine Maker - More Trial, Less Error
Summary: The pressure for increased efficiency pervades the pharma industry, including the clinical trials sector, where traditional supply models can lead to overstocking, waste and higher costs. This article, originally published in "The Medicine Maker" explores if there is a more effective supply strategy...
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eBook
Comparator Sourcing
Summary: Pharmaceutical companies face a number of challenges when sourcing comparator compounds for clinical trials, including addressing product lead times, availability, expiry limitations, safety or cost. This eBook illustrates how clinical trial sponsors can determine the best strategy to meet these challenges...
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Webinars
Optimizing Your Clinical Supply Chain Strategy For Asia-Pacific Studies
Summary: Unlike Europe where clinical trial regulations are largely standardized between the EMEA member states, no such organization or harmonization exists in the APAC region, making conducting multi-country studies within the region much more complex for clinical sponsors, particularly with regards to the sourcing...
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eBook
Clinical Trials Innovations
Summary: Developing, implementing, and managing a clinical trial involves coordination of multiple factors in an ever-changing environment. Recent innovations in trial design and management including a demand-led approach to drug supply, adaptive trial design, mHealth for patient-centric and site-centric trials...
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Webinars
Maintaining Product Integrity In Biologic & Biosimilar Clinical Studies
Summary: Specialized expertise in cold chain shipping and logistics are critical to avoid costly delays and potential for patient harm resulting from an interruption or delay in necessary clinical supply. Maintaining product integrity and reliability of supply can be especially challenging for biologic and biosimilar studies as the investigational...
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Webinars
Identifying & Addressing The Hidden Root Causes Of Supply Chain Inefficiency
Summary: Delayed. Out of stock. Over-budget. Unavailable…All words that clinical trial sponsors never wish to hear in reference to the impact of supply chain performance on their study. And yet, considering the critical role the supply chain plays, it has surprisingly remained largely unchanged for several decades...
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Webinars
Around The World In Clinical Trials: New Regulations & Country Specific Challenges
Summary: While thorough knowledge of a country’s regulatory requirements is critical, understanding both the written and unwritten regional differences and business practices that come in to play that can make the difference between clinical supplies moving successfully between countries, being detained in Customs...
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Article
Around The World In Clinical Trials: New Regulations & Country-Specific Challenges
As certain regions of the world are added to a clinical study, the logistical and regulatory challenges associated with clinical trial supply distribution can rise exponentially. While having thorough knowledge of a country’s regulatory requirements is critical, understanding both written and unwritten regional rules...
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