Clinical Data Repository Benefits for Early Adopters

posted on 30th September 2015 in Data Talk

Clinical data repositories (CDRs) are a hot topic among clinical trial data managers. CDR’s empower data managers, and other employees who utilize data in the organization, to control all their data in real time. Consolidating data from varied sources and allowing us to see the data in a unified view is a dream come true. […]

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The Challenges and Goals of Data Standardization

posted on 17th September 2015 in Data Talk

The processes surrounding data collection, transformation and analysis continues to be unstable and inconsistent in the life sciences industry. In recent years, data standardization practices have been developed and honed to fight these inefficiencies. With the right people using the right tools, standardization can improve clinical trial research through enhanced data quality, integration and reusability. […]

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How To Support Electronic Data Capture

posted on 10th September 2015 in Data Talk

  At eClinical Solutions we combine technical and clinical experience when helping life science companies design and implement an electronic data capture (EDC) system. We’re involved every step of the way, offering support from start to finish. Through the Medidata Clinical Cloud, we offer organizations an industry-leading technology that not only supports EDC, but also […]

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Consider Medical Coding During the Clinical Trial Study Build

posted on 2nd September 2015 in Data Talk & Recommendations

I’ll be honest, medical coding clinical trial data is a time-consuming job requiring attention to detail that some might describe as tedious. However, it is critically important in ensuring the data collected as a part of clinical trials can be quickly analyzed for results and insights. As clinical data arrives from around the world, clinical data managers […]

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How the Clinical Trial Experience is Improving

posted on 27th August 2015 in Data Talk

Clinical trials play a big role in the development of pharmaceuticals to treat diseases and improve people’s health across the world. It’s in everyone’s best interest to improve clinical trials however we can. Improving efficiency, cost and accessibility will allow more people to get the treatment they need at a lower cost. Putting patients in […]

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The 3 Biggest Factors Changing Clinical Trials Today

posted on 20th August 2015 in Data Talk

Professionals in the drug development world know that clinical trials are expensive. In fact, they’re the most costly part of getting a drug on the shelves. Yet, only a slim percentage of these drugs actually make it through the clinical trial phases. As clinical development becomes more complex and regulations even more strict, there is […]

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How Medidata Rave Increases Clinical Trial Flexibility

posted on 13th August 2015 in Data Talk

eClinical Solutions is an avid partner with Medidata, and we’re experts when it comes to the ins-and-outs of the Medidata Rave electronic data capture (EDC) and clinical data manager platform. Rave is part of Medidata’s Clinical Cloud, which makes data capture, management and reporting easy. We’ve worked with several clients to implement Medidata Rave while […]

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Five Key Attributes for Maintaining High Performing Teams

posted on 30th July 2015 in Recommendations

I am fortunate to have worked with some great teams in my career, and it’s a great feeling when teams work well together and accomplish high-level goals. As a senior leader at eClinical Solutions, it’s my job to hire good people and to create an environment where they can grow and succeed. I ran across […]

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elluminate: The Foundation for Complete Data Standardization

posted on 23rd July 2015 in Data Talk

Data and analytics are two of the biggest buzzwords in the Life Sciences industry today. While we’re creating exponentially more data points than we have in the past, they are virtually useless if they cannot be read and analyzed. This is a common problem that is found throughout the clinical trial community. The first step […]

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How Clinical Data Integrity and Quality Help Achieve GCP

posted on 16th July 2015 in Recommendations

Good clinical practice (GCP) is a foundational element in conducting clinical trials. According to the FDA, “GCP is an international ethical and scientific quality standard for designing, conducting, recording, and reporting trials that involve the participation of human subjects. Compliance with this standard provides assurance that the rights, safety, and well-being of trial subjects are […]

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