Are you optimizing
clinical intelligence?

The right data and strategic insights are often elusive. That is why MDCPartners takes deeper dives for our clients in the pharmaceutical and medical industries. By merging our business expertise with unique IT platforms and portals we can fully support your intelligence and business needs for clinical trial optimization, medical expert identification, and regulatory compliance.

Strategic data advances clinical development

MDCPartners is dedicated to providing tools and services to help pharmaceutical companies make better decisions. Our flagship product, ta-Scan, is a web-based data platform that helps users monitor, aggregate, and analyze regulatory data, trial data, and expert profiles. Whether you need to optimize study placement, select research partners, or manage your portfolios, our products and portals will help you bridge the information gaps in today’s competitive clinical research environment.

Learn more about ta-Scan Visit ta-Scan.com

While ta-Scan offers the premier navigation and data search experience, MDCPartners has additional data visualization tools that can provide support for more specific needs.

CTAR – Custom reporting for ta-Scan

This complementary tool supplements your ta-Scan data searches and analyses by generating customized reports that are automatically updated with each weekly ta-Scan data refresh.
Learn more about CTAR


LifeRhythm – Visualizing data relationships

Another complementary ta-Scan tool is LifeRhythm, which displays data in an appropriate visual context with interdependent variables. So, for example, you can search for the interconnectivity of any leading researcher.
LifeRhythm also provides a quick method for visualizing the origins of scientific papers, so one publication can connect users to others who have presented on the same topic or participated in related trials. LifeRhythm also includes a robust event dashboard, which tracks recent data revisions.
Learn more about LifeRhythm


Alesia – Advanced Gantt charts

This complementary platform allows ta-Scan users to depict specific clinical trial analyses as advanced Gantt charts.
Learn more about Alesia

Are your medical devices meeting standards?

To support manufacturers of medical devices and in vitro diagnostics (IVDs), MDCPartners has developed normScan, a web-based standards tracking tool tailored to your product range. It can also help you obtain regulatory approval for marketing products throughout Europe, and can assist you with a broad spectrum of regulatory issues related to maintaining compliance.

Learn more about normScan Visit normScan.com

Bring your own data, use our know-how

MDCPartners doesn’t just offer tools for visualizing public data. We also provide tools for depicting external client data merged with information from our public data cloud. So if you have specific needs that surpass the scope of ta-Scan, you can still rely on us for tailor-made data solutions.

Learn more

Latest News & Events

MDCPartners ta-Scan 5 SCOPE 2017 Miami Florida

Discover ta-Scan 5 at SCOPE 2017

Summit for Clinical Operations Executives

It’s never too early for good Year’s resolutions! Ours? Start off 2017 with a bang! Indeed, in January 2017, MDCPartners will travel to sunny Florida again for the yearly Summit for Clinical Operations Executives (SCOPE), and it goes without saying that we are already looking forward to it.

The 8th Annual SCOPE Summit, taking place January 24-26, 2017 in Miami, Florida in the Hyatt Regency, will offer three stimulating days of in-depth discussions in 13 different conferences, 6 pre-conference workshops and 2 symposia focused on issues related to each aspect of clinical trial planning and management: Data Integration, Feasibility, Site Selection and Management, Patient Engagement, Recruitment and Retention, Mobile Tech, Project Management, Outsourcing, Forecasting, Budgeting and Contracting, Quality (QbD) in Trial Conduct, Risk-Based Monitoring, Post-Marketing Studies, Observational Research, Clinical Lab Services, Precision Medicine and Biomarker-Driven Trials. View SCOPE’s programs here.

Introducing ta-Scan 5

ta-scan 5 scope 2017

Our business and IT teams will present the clinops experts at SCOPE ta-Scan‘s latest version we have been working on the last months: ta-Scan 5! This update includes a lot of new features and a complete style make-over to enhance the user experience. Join us in Miami to discover how our clinical business intelligence software and our public-private data integration skills can leverage today’s clinical big data challenges.

If you want to get a live demo of ta-Scan 5 and learn more about our software solutions, visit us at booth #702-704 or make an appointment with our CSO David Cocker, Director of Business Development USA Matt Tumasz, or Technical Product Manager Kristof Geentjens.

The ta-Scan clinical business intelligence team at SCOPE 2016
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MDCPartners and ta-Scan at Big Data in Precision Medicine 2016 Washington, D.C.

MDCPartners Innovation Partner Big Data in Precision Medicine Washington

Big Data in Precision Medicine

With ESMO 2016 coming to a close in Copenhagen, MDCPartners is getting ready for their next stop: we are this year’s Innovation Partner of the Big Data in Precision Medicine meeting, which will take place in the Capital Hilton in Washington, D.C. on November 1-2, 2016.

This meeting attracts 250-300 senior executives from across the drug development sector including Big Pharma, biotech, leading solution providers, government, healthcare and academia. The meeting addresses the opportunities and challenges of big and real-world data, and how machine learning and cognitive computing can be applied in the context of drug development. View the meeting’s streams and the meeting agenda here.

Private Clinical Trial Data in the Real-World Data Context

On Tuesday November 1 at 9:30 AM, MDCPartners’ Chief Scientific Officer David Cocker will present our findings on “The value case of private pharma clinical trial data in the real-world data context”.

Real-world data (RWD) is generally the term used to refer to any data which is collected outside of randomized clinical trials (RCT). The data can be from sources including patient data from hospitals and clinicians. The premise is that RWD combined with information from RCTs can provide better research outcomes and improved healthcare.

Unfortunately, available clinical trial information data is really not that big. Often it is also dispersed and contradictory, and includes duplicates through multiple entries that are not verified and/or matched. Many transformative actions with data are frequently heralded as a big data panacea long before any analytical conclusion can be applied.

This presentation will explore the challenges faced when approaching the question of clinical trial data merging and its interoperability with public clinical trial data for creating valuable insights for study placement.

Meeting Up

ta-Scan’s data team will be present in Washington, D.C. as well to show the precision medicine experts how our clinical business intelligence software ta-Scan can leverage today’s medical big data challenges.

If you want to learn more about our software solutions, you can meet us personally during the exhibition at booth #1 or make an appointment with CSO David Cocker or Strategic Data Analyst, Oncology Jonathan Crowther.

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MDCPartners and ta-Scan at ESMO 2016 Copenhagen

Meet the ta-Scan Oncology Team at ESMO 2016 in Copenhagen

European Society for Medical Oncology

Next stop on our bill: the ESMO 2016 Congress in Copenhagen, Denmark on 7-11 October 2016.

The annual ESMO congress is the premier scientific platform to present your oncology research and as such, the ultimate learning experience for congress attendees. Across disciplines and across cultures, ESMO bridges the gap between researchers, clinicians and patients and unites all stakeholders focused on finding the most effective cancer treatment solutions available today.

ESMO 2016 will continue to build upon the success of past congresses, offering a top-notch scientific and educational programme created by international experts in oncology. View the online meeting programme here.

Meeting up

ta-Scan‘s oncology team will be present in Copenhagen as well to show the oncology society how our clinical business intelligence software ta-Scan can leverage today’s medical oncology data challenges.

If you want to learn more about our software solutions, you can meet us personally during the conference. Just make an appointment with David CockerJonathan Crowther, or Koen Snijders.

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Downloads

  • ta-Scan's Trial Feasibility Wizard

    More information about ta-Scan's Trial Feasibility Wizard in this fact sheet.

    US Letter Format | A4 Format
  • ta-Scan for Expert Profiling & Exploring Disease Landscapes

    Learn how to use ta-Scan for expert profiling and exploring disease landscapes.

    US Letter Format | A4 Format
  • ta-Scan for Competitive Intelligence & Medical Affairs

    Learn how to use ta-Scan for competitive intelligence and medical affairs in this fact sheet.

    US Letter Format | A4 Format
  • ta-Scan for Clinical Trial Planning & Optimization

    Learn how to use ta-Scan for clinical trial planning and optimization in this fact sheet.

    US Letter Format | A4 Format
  • ta-Scan's Research Landscape Comparison Wizard

    More information about ta-Scan's RLC Wizard in this fact sheet.

    US Letter Format | A4 Format

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