Are Your Cloud Computing Systems Compliant and Validated?

posted on 20th November 2014 in Data Talk

In a recent blog post my colleague Sam Anwar, our VP of Engineering, shared that life sciences companies have an opportunity to accelerate adoption of cloud computing and software-as-a-service (SaaS) IT models to accelerate new product development, improve patient outcomes, and enable expansion into new markets, all while reducing costs and creating a more agile […]

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5 Steps to Integrate External Data into Your EDC Platform

posted on 10th November 2014 in Solutions

Frequently clients reach out to us for help with a process to integrate and manage clinical trial data from partners and external sources such as labs. Siobhan Raynard, one of our Clinical Data Managers, and I put together the list below of five key points to consider when putting together a plan to manage the […]

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Can the Life Sciences Industry Adopt Cloud Computing?

posted on 10th September 2014 in Solutions

Life sciences companies are adopting cloud computing and software-as-a-service (SaaS) IT models, particularly in the areas of sales and marketing. There is an opportunity to extend the cloud’s impact into areas such as R&D and supply chain. However, there are legitimate concerns about protecting intellectual property and demonstrating compliance with industry regulations. The primary two […]

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How Can Electronic Data Capture Support Risk-based Monitoring?

posted on 10th April 2014 in Solutions

As clinical trial sponsors are looking to shift from traditional clinical trial monitoring approaches to risk-based monitoring, an electronic data capture (EDC) system is a key component. An electronic data capture system supports risk-based monitoring by: Dynamic assignment of source data verification Empowering central monitoring of clinical trial data An EDC system, such as Medidata Rave, […]

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Can Clinical Trials Benefit from Both EDC and CDR Technologies?

posted on 27th March 2014 in Solutions

There are times when our clients need to collect and aggregate date from their clinical trials, and also gain meaningful insights from clinical trial data that can help them make better decisions. In these situations we work with our clients to implement an electronic data capture (EDC) and a clinical data repository (CDR) platform. Our […]

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C-Suite Views on Opportunities and Barriers for Clinical Services

posted on 16th January 2014 in Partners

Recently PharmaVOICE asked me and other C-Suite executives from around the clinical services ecosystem what we see as opportunities and barriers for improving the clinical development process. I’m excited about the promise of genomics as an opportunity to innovate the process, which can lead to increased success and decreased costs. The January 2014 issue of […]

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Are You Ready to Move Your Clinical Trial Processes to the Cloud?

posted on 13th December 2013 in Solutions

Life science companies are struggling to enhance the productivity of their R&D processes. A new paradigm is emerging that moves the conduct and management of clinical trials to cloud-based applications. With cloud-based technologies, sponsors can implement an end-to-end data management strategy to transform their clinical development life cycle processes including data acquisition, storage, aggregation, and […]

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Leverage Technology For Data Aggregation from Disparate Sources

posted on 14th November 2013 in Solutions

Sponsors are facing intense pressures to change the way clinical research is conducted in order to decrease costs and speed up the research and development process. Equally important data management challenges are: 1) The ability to enhance data sharing between partners such as study sites, CROs, clinical trial monitors, and development partners such as small or […]

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