6 Things That Differ Between Industry-Initiated and Academic Clinical Trials

By Clinical Trial Management, Health Care Research No Comments

Clinical trials are fundamental to testing new medicine, investigating existing medicine and improving healthcare. Most research protocols are either designed by researchers employed by the pharmaceutical/ medical device company or investigators from academic institutions. Here are six things that distinguish industry clinical trials from academic clinical trials: Funding – Industry-initiated clinical trials are financially supported by the industry. The primary…

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3 Packaging Decisions You Can Make to Improve Clinical Trial Compliance

By Clinical Trial Management, Outsourcing, Packaging and Distribution No Comments

Study non-adherence is an ongoing problem surrounding clinical trials. Noncompliance drives up research costs and increases the time it takes new medicines to make it to the market. One study suggests that costs associated with noncompliance are as high as $1.5 billion by the time the investigational product (IP) is fully developed 1. Considerate IP packaging is one way researchers…

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Brexit and the Future of Clinical Trials in Europe & the United Kingdom (UK)

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In 2016 the United Kingdom (UK) held a national referendum in which the country voted to leave the European Union (EU). Since then, the UK and the EU have been negotiating an agreement that outlines the terms of the UK’s withdrawal. With uncertainty about the terms on which the UK will leave the EU, it is important to consider how…

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What Does a Successful Cold Chain Look Like?

By Clinical Trial Management, Cold Chain, Health Care Research, Packaging & Distribution, Supply Chain No Comments

Clinical supply chain logistics are constantly changing as new technologies and developments are adapted. While multiple factors are responsible for reshaping the clinical trials logistics landscape, the explosive evolution of biologics is the key driver. In order to preserve the integrity of biologics and other highly sensitive medicinal products, as well as maintain the validity of trial results, cold chain…

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Reducing the Cost of Clinical Trials

By Clinical Trial Management, Outsourcing, Technological Advancements No Comments

Finding ways to improve efficiencies and manage the increasingly uncertain and complex clinical trial supply chain is a high priority for the pharma and medical technology industry. Annually, $20 billion of R&D spending is essentially wasted due to poor clinical trial management and planning. Based on our experience with supply chain logistics management, we have identified some innovative approaches and…

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3 Steps for a More Sustainable Clinical Supply Chain

By Clinical Trial Management, Packaging & Distribution, Supply Chain, Sustainability No Comments

Over recent decades, the heightened awareness of sustainability issues among consumers, combined with the prevalence of corporate social responsibility and an increase in regulatory standards, has put pressure on the clinical trial and pharmaceutical industry to reduce the environmental impact of its activities. The potential benefits from creating a greener clinical supply chain includes an enhanced brand reputation and operational…

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5 Things You Need to Know About Clinical Trial Drug Packaging

By Clinical Trial Management, Drug Waste, Health Care Research, Supply Chain No Comments

Packaging is an important component of successfully getting a drug ready for its clinical trial. While there are a number of regulations surrounding drug packaging and labeling, packaging specialists have one of the most creative roles in the clinical trial industry because of unique and specific packaging needs. In this article, we break down the five most important aspects of…

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Patient Enrolment Retention in Clinical Trials

By Clinical Trial Management No Comments

In order to successfully run clinical trials, you will need to be able to successfully recruit subjects. It is critical to the success of your trial to implement strategies for subject recruitment and retention.  At the subject level, participation is voluntary based on informed consent. An essential element of the informed consent process is ensuring that subjects are provided with comprehensive…

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5 Risks Most Clinical Supply Professionals Overlook

By Clinical Trial Management, Supply Chain No Comments

Risk-awareness is a critical component of successful clinical supply management; you cannot fix the problems you don’t know about. We see clinical supply professionals overlooking the same key risks time and again. Let’s address them now. Expiry dating One of the biggest impacts to the success of clinical supply management is expiry dating, particularly of the product itself. As formulation…

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