From Convergence Vision to Reality
Technology convergence is the engine for the next generation of eClinical platforms. What’s needed is a unifying architecture that blurs lines between applications, enriches the user experience, and integrates easily with external tools and partners. Perceptive Informatics’ MyTrials eClinical platform – built upon best-of-breed technology – accomplishes these goals. Whether used on its own or in a mixed environment with client technology, MyTrials delivers the scientific and business benefits of convergence today. Learn more about the foundational technology underpinning MyTrials and the benefits MyTrials delivers.
Comply or Perish: Maintaining 21 CFR Part 11 Compliance
The biggest challenges of Life Sciences companies today are maintaining a robust product pipeline and reducing time to market while complying with an increasing and evolving multitude of Federal and international regulations. In this paper, we discuss the particular requirements of rule 21 CFR Part 11 and describe how OpenText Regulated Documents built on OpenText Content Server – the leading collaborative knowledge management software from OpenText, enables Life Sciences companies to comply with 21 CFR Part 11.
Enterprise Informatics: Key to Precision Medicine, Scientific Breakthroughs, and Competitive Advantage
In recent decades, finance, retail, and other industries have revolutionized the way they do business by taking advantage of the transformative power of aggregated data and implementing large-scale automation. Meanwhile, the healthcare industry has lagged behind. Why? And when will healthcare finally be able to make progress on an equally game-changing level?
NOW, answers this Remedy Informatics white paper, which explains how recent technological advances allow healthcare delivery and life sciences research organizations to leverage their data in powerful new ways. Optimal use of these innovations will result in better decisions, faster discovery, greater productivity, and higher-quality patient care and outcomes enterprise-wide.
Bridging the gap between compliance and innovation
ENOVIA PLM solutions for life sciences
Success in medical device manufacturing requires continual innovation in order to deliver improvements while complying with the extensive quality systems regulations. Product development and regulatory compliance functions are usually conducted by different organizations in silos, consuming excessive amounts of time and less than optimal results. The ENOVIA® product lifecycle management (PLM) solutions for life sciences offer an end-to-end solution within a single environment, spanning the entire product development process as well as most of the quality systems processes. Contributors within the different groups can easily access the information they need and workflows can be developed within both product development and regulatory compliance. The result is dramatic time-savings and errors reduction in both product development and regulatory compliance.
This whitepaper is provided complimentary courtesy of Persistent Systems, a value-added reseller for Dassault Systèmes' PLM Solutions. Persistent Systems is a global company specializing in software product and technology services. Persistent focuses on developing best-in-class solutions for life sciences, medical device, and healthcare verticals and provides unmatched services for implementing, upgrading and optimizing Dassault Systèmes' (PLM) solutions. www.persistentsys.com
Clinical Project Management Survey
In October 2013, Clinical Informatics News conducted a survey within the biotechnology and pharmaceutical sector on Clinical Project Management. The purpose of the study was to determine how clinical project managers see the globalization of clinical trials, what challenges they face, what tools they believe will help them, as well as their budget predictions for 2014. With 356 respondents the study is projected to carry a margin-of-error under 2%. Download the results today!
Outsourcing Clinical Trials Survey
In October 2013, Clinical Informatics News conducted a survey within the biotechnology and pharmaceutical sector on Outsourcing Clinical Trials. The purpose of the study was to determine which areas of clinical trials are outsourced,the challenges faced, and why companies make the decision to outsource. Download the results to see what your colleagues are saying about outsourcing clinical trials.
Clinical Trial Management Systems Survey
In January 2013, Clinical Informatics News and BioClinica conducted a survey within the biotechnology and pharmaceutical sector on Clinical Trial Management Systems. The purpose of the study was to determine how clinical trial management systems are used, what types, and for which purposes as well as the processes used within the organizations of the respondents.
2013 Annual Life Sciences IT Survey
This exclusive survey is the first in an annual series of reports in which we will diagnose key trends in the life sciences IT space by interviewing key opinion leaders in the industry.
Survey on Clinical Monitoring
The Cambridge Healthtech Media Group, along with Clinical Informatics News and Barnett Educational Services conducted this market survey on Clinical Monitoring in August 2012. Download the results here.
Survey on Electronic Data Capture
The Cambridge Healthtech Media Group, along with Clinical Informatics News and Barnett Educational Services conducted this market survey on EDC in September 2012. Download the results to see what your colleagues are saying about EDC.
Clinical Trials Survey
CHI Professional Marketing Services, in conjunction with Bio-IT World and Clinical Informatics News conducted this market survey on Clinical Trials in August/September 2011. This brief survey was intended to provide insight into three areas:
• Key clinical process challenges facing the industry
• Trends in cloud computing usage and projected growth within
the clinical sector
• Usage of outsourced services, and projected growth
Download the results here.
Recent whitepapers include:
To promote your whitepaper with Clinical Informatics News or Bio-IT World, please contact:
Jay Mulhern, Manager, Business Development at 781-972-1359 or firstname.lastname@example.org