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CTMS

Removing Risk from Clinical Trial Management System (CTMS) Implementations

Upcoming Webinar: Removing Risk from Clinical Trial Management System (CTMS) Implementations

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  • 15 Nov

Join us for our upcoming webinar on November 28th during which Justin Hunt, Director of CTMS Implementation Services at Bioclinica, Inc., will present and discuss a case study providing insight into the benefits realized by a contract research organization (CRO) purchasing a CTMS who started with a small, limited implementation.

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CTMS and RBM: Hot Topics at OCT Nordics in Copenhagen

CTMS and RBM: Hot Topics at OCT Nordics in Copenhagen

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  • 24 Oct

The 5th Annual Outsourcing in Clinical Trials (OCT) Nordics conference provided another outstanding opportunity to explore a beautiful city, stay in the world’s greenest hotel and gain additional insight into aspects of clinical trials that are important for my daily work and even those that don’t touch my daily eClinical life. The mix of representatives from long-established pharma, CROs, biotech and third-party vendors enabled refreshing conversations about how we can work together to improve our communication and move in synergy toward our shared goals.

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Realize the Benefits of a Fully Developed CTMS Without the Typical Time to Implement, Using OnPoint Direct CTMS

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  • 25 Apr

In our experience, many small- to mid-sized companies view the implementation of a Clinical Trial Management System (CTMS) to be too resource-intensive (finances, time and human resources); because of this and other reasons, many of these companies compromise with systems comprised primarily of manual processes using spreadsheets, half-built internal systems or less-than-ideal implementations. However, CTMS plays an integral role in the conduct of your trials, and the implementation should support your specific needs.

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Introducing OnPoint Direct, Bioclinica's Powerful Rapid Startup CTMS

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  • 19 Jul

With thousands of people, hundreds of investigative sites, multiple CROs and various eClinical source systems—all generating massive amounts of data—clinical trials are an enormous undertaking. While leading organizations use Clinical Trial Management Systems (CTMS) to centralize operational data and automate processes so they can make better decisions, a CTMS can be out of reach for many small to mid-size companies, leaving them with isolated spreadsheets and/or inefficient, manual practices.

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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

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

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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Bioclinica is organized into three business segments so that we can provide expert service and multifaceted technologies. Our Medical Imaging & Biomarkers segment includes an Imaging Core Lab, a Cardiovascular Safety division, and a Molecular Marker Laboratory. Our eHealth segment comprises eClinical Solutions, Randomization & Trial Supply Management, Safety & Regulatory Solutions, and Financial Lifecycle Solutions. Under the Global Clinical Research segment, we offer a network of research sites, patient recruitment, and a Post-Approval Research division.

What's next from Bioclinica? Hear if first during #PCTrials Europe next week in Amsterdam! https://t.co/ICngaxA9mg https://t.co/SXxPj3NpD2
bioclinica (5 hours ago)
Join Bioclinica's Justin Hunt on Nov. 28 in a live webinar! Find out how to overcome common hurdles in CTMS impleme… https://t.co/wHfWHtI7sj
bioclinica (Yesterday)
Another CRO seeing big gains in the sites payments process! Access the Case Study here https://t.co/jsCxhmKcLo https://t.co/LpIKEtBKtE
bioclinica (Yesterday)
Great advice from our Dir. Cardiovascular Imaging on quality imaging acquisitions & assessments in clin trials. https://t.co/OVH7pZ3SL0
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Almost here! #PCTrials Pre-arrange a meeting w @bioclinica Drop by & s/w David Kiger & Mike Lange. Mike will give a… https://t.co/8ymd2Q9KcJ
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Almost here! #PCTrials Pre-arrange a meeting w @bioclinica Drop by & s/w David Kiger & Mike Lange. Mike will giv… https://t.co/MpxTDV1T1L
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Latest Blogs:

Removing Risk from Clinical Trial Management System (CTMS) Implementations
Collaboration Between Clinical Operations and the Logistics and Supply Chain Teams is Key to Trial Success
The Value of Protocol Review
CTMS and RBM: Hot Topics at OCT Nordics in Copenhagen
Congressman Meehan and Bioclinica CEO John Hubbard at recent visit to Bioclinica's Audubon offices