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CTMS Market Dynamics And Service Provider Benchmarking
In this report, ISR surveyed 110 qualified CTMS decision makers regarding their insights on topics such as CTMS selection drivers, outsourcing trends, use, and perceptions of providers. Respondents also shared general improvements they would like to see in the next generation of CTMS software and conveyed provider-specific advantages and improvement suggestions for their preferred system. You can purchase the full report or download a free preview by clicking here.
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Inspire Awards Honor The Industry’s Best
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By Ed Miseta, chief editor, Clinical Leader
The DIA Inspire Awards have grown every year that Barbara Lopez Kunz, global chief executive for DIA, has been with the organization. Kunz, who has been with DIA since 2013, notes it has become the place to be for attendees traveling to the annual meeting.
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Getting A Handle On Clinical Trial Costs
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By Amit Pratap Singh Rathore, principal analyst, Beroe Inc.
Recently, clinical trials have become very complex affairs, especially for small and medium biotech companies. There are many factors behind this, including, but not limited to, increased costs and regulatory requirements. According to Tomasz Sablinski, CEO at Transparency Life Sciences, the cost of clinical trials increased by around 100 percent from 2008 to 2019. A study published in JAMA Internal Medicine in 2018 found that out of 138 pivotal trials assessing 59 new therapies that received FDA approval between 2015 and 2016, there was a more than 100-fold difference in the costs of clinical trials.
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eConsent Resources Overview
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Article
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By Jackie Brusch,
CRF Health, a CRF Bracket Company
Access to electronic eConsent resources from the past twelve months.
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Advancing A Diabetes Multiregistration Program
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Case Study
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Covance
A large pharmaceutical company asked Covance to support their studies for a diabetes Phase 3 program specifically to register a drug to treat type 2 diabetes. Read how Covance utilized its rich central laboratory services database and helped the sponsor achieve first patient in (FPI) ahead of schedule for all studies in the program and beat historical industry performance across a number of key metrics.
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Minimizing Errors And Saving Time In Drug Receipt Processes
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Case Study
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Thermo Fisher Scientific
The speed/accuracy tradeoff is a well-known phenomenon in psychology for processes requiring human input: The faster you go, the more likely it is that errors will be introduced into the system. This presents a major challenge for complex supply chains that demand both efficiency and accuracy. This case study shows the steps Fisher Bioservices took to improve efficiency and accuracy to combat the complexities of the drug receipt process.
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| Life Science Leader Magazine |
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Have you heard of Life Science Leader?
Check it out today for access to candid interviews with top-tier executives on how they do business.
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