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Governance and Collaboration: CTMS Checklist

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  • 02 Mar

A recent market research report forecasts that the eClinical solutions market will be worth 5.98 billion (USD) by 2020. With sponsors and CROs adopting new eClinical software, or replacing legacy systems, such as clinical trial management systems (CTMS), vendors are emerging with new software to stake a claim in this growing market.

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The Future of Clinical Trial Data Management and Technology's Growing Impact

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  • 22 May
At BioClinica's 2015 Global User Conference, I had the pleasure of leading an expert panel discussion on the future of data management. I would like to share some highlights from my perspective. Panel participants were Daun Bahr, senior director data management Orexigen; Queennette Santiago, head of data management Ultragenyx; Clara Plascencia, associate director of clinical data management Pharmacyclics; and Ann Seibel, clinical data manager BioClinica.
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Practical Risk Based Monitoring Methodologies

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  • 17 Mar

Putting RBM methodologies into practice

eClinical Greetings from Barcelona!
Jonathan Andrus
After a few crimps in the travel plans thanks to another winter storm hitting the US, everyone arrived safe and sound in sunny Barcelona for our second Annual European User Conference. It was two days of quality time with our customers and partners (recapped here in a news release).

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CTMS Microsoft SharePoint Integration Key to CROs

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  • 12 Mar

CTMS: Microsoft SharePoint Integration
When surrounded by such beauty and energy in Barcelona, who wants to sleep? Having just returned from BioClinica's European User Conference there last week, I admit I'm still reacclimatizing to the UK as I write this.

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Site Monitoring Reinvented Part 2

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  • 02 Mar

The Making of an MVR with Microsoft Office Smarts and an Iron-Clad Audit Trail

Regulatory authorities require clinical trial progress to be monitored. The site visit report, known as the Monitor Visit Report (MVR), is where sponsors provide evidence that all regulated activities have been completed along with documentation of the outcome. These reports are open to regulatory inspection at any time during a study, as well as after, and even post product approval.

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Make clinical trial management faster and easier

Clinical Trial Management: If I Only Knew Then What I Know Now

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  • 06 Feb

Can we make our data collection faster and easier? Will the right treatments be onsite when it's time to randomize? How can we be certain that problems identified at sites are being resolved?

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CTMS & eTMF seamless integration at ShareFEST 2013

The New Wave of CTMS: Reduced Frustration through Seamless Integration

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  • 21 Mar

We've recently heard quite a bit of industry conversation regarding the touch-points between clinical trial management systems (CTMS) and electronic trial master files (eTMF).  In addition to this blog post, we will be discussing this evolving topic in greater depth at the upcoming ShareFEST 2013 conference in Philadelphia, April 25 and 26.  While there are many questions concerning the integration of CTMS and eTMF, they can typically be boiled down to these:

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Clinical trial management on Microsoft Surface

Clinical Trial Management on a Microsoft Surface

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  • 25 Oct
There have been several tablet announcements this week. But, one of these announcements is vastly different than the others. It’s not an updated model or a smaller redesign of an existing product. It’s a brand new concept in tablet computing, and is available today. It’s the Microsoft Surface, and its innovative hardware and software have the potential to change the game in clinical trial management.
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CTMS and eTMF in Harmony

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  • 20 Jul
There have recently been a lot of industry conversations regarding the touch-points between clinical trial management systems (CTMS) and Electronic Master Trial Files (eTMF). While there are many questions concerning the integration of CTMS and eTMF, they can mostly be boiled down to the following three:
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2012 Microsoft Life Sciences Innovation Award

OnPoint CTMS Monitor Visit Report Wins Microsoft Award

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  • 11 Jul

It's always fun to meet new people at DIA and see what new products and innovations are being offered by our compatriots in the eClinical field. Plus it offers me the opportunity to demonstrate BioClinica's products to a lot of people without traveling across the country. No surprise, the big hit this year was our Express EDC and OnPoint CTMS Metro apps running on a tablet using the upcoming Windows 8 operating system from Microsoft. I can't wait until the WIN8 release!

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Powerful Clinical Apps

Windows 8 and Surface Tablet Pave the Way for Powerful Clinical Apps

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  • 21 Jun

The internet is buzzing over the news that Microsoft is entering the tablet market. Anyone who follows such things knew that Windows 8 would have touch interface designed for tablets, but few were expecting Microsoft to produce its own hardware to run it. Since BioClinica is a Microsoft Life Science Gold Certified partner our developers have been running Windows 8 on tablets for the past few months. I can’t wait to get my hands on one! I really like that the Windows OS on the slate is the same as on the PC so I am not limited to running only ‘tablet based’ clinical apps.

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CTMS Software Clinical Trials

Streamline Clinical Trial Process with OnPoint CTMS Software and eTMF

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  • 24 May
Remember the board game Mouse Trap? How each piece of the trap triggered an action that set off the next part of the trap? Well, BioClinica and NextDocs are bringing this concept to clinical trials by extending integration that unites BioClinica's OnPoint Clinical Trial Management System (CTMS) and NextDocs Electronic Trial Master Form (eTMF) products.
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BioCure Monitoring Trip Report

Site Monitoring Goes High Tech with On and Off Line CTMS Forms

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  • 20 Apr

Do you still carry a briefcase full of paper? Are you lost without an internet connection? Hopefully, you have embraced technology and answered "No" and "Yes" to those questions.

Here in 2012, most clinical studies use electronic data collection (EDC). The use of Clinical Trial Management Systems (CTMS) to perform site management and keep track of study regulatory documents, monitoring visits and study budgets has been significantly on the rise over the past few years. Using paper envelopes to randomize is almost extinct and study monitors are finally ready to part with their big suitcase of highlighters, black pens, 3-part NCR forms, and yellow sticky notes.

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Information Brief at Alzheimer's Association Gala in Washington, DC

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  • 20 May
Following on the theme of Alzheimer’s disease, there is a great summary paper from last month on the facts and figures (1) of this disease. Much of this was used as the information brief at the Alzheimer’s Association Gala in Washington, DC. Some of the facts are quite surprising, e.g. it is estimated that 5.4 million Americans have AD. Every 69 seconds someone in America develops Alzheimer’s disease. Total payments in 2011 for health care, long term care and hospital services for people age 65 years and older with AD and other dementias are estimated at $183 million.
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The Value of Using Microsoft Office Products in CTMS Systems

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  • 15 Feb

There has been quite a lot of discussion within the clinical trial management industry regarding new improved CTMS and study setup products. These new CTMS solutions all seem to focus on updating the traditional model with a slick, user-friendly interface as well as overall improved functionality (which is great). However, in my experience, truly elegant CTMS product design taps directly into peoples’ existing framework and understanding, reducing the learning curve to a flat line.

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