ERT Demonstrates Patient Safety Expertise in Clinical Trials with New Knowledge Series of Papers
PHILADELPHIA, Jan. 14 ERT (Nasdaq: ERES), a leading provider of centralized services to the biopharmaceutical, medical device and related industries, today announced its new ERT Knowledge Series of educational papers, written by ERT experts. Each paper discusses issues relevant to patient safety in clinical trials today and further establishes ERT as an experienced and reliable partner in products and services for the clinical trials industry. The papers are now available to download from the company's website - www.ERT.com.
This new Knowledge Series of papers focuses on two of ERT's most innovative patient safety solutions, the centralized collection and analysis of ECG data to ensure cardiac safety in clinical trials and the use of electronic patient reported outcomes (ePRO) for suicidality monitoring in clinical trials. ERT's proven cardiac safety solutions offer a centralized method of accurate ECG data collection and analysis. Its centralized core laboratory enables the real-time collection of consistent and reliable ECG data -- a critical element in the accurate assessment of the cardiac effect of new drugs. Centralization not only minimizes inconsistencies that may occur from site to site but also reduces clients' workloads. ERT simplifies ECG data management and analysis to provide on-demand, real-time access to ECG study data.
Clinical trials can be delayed due to slow enrollment, problems with paper documentation and the inability to monitor sensitive patient data, costing sponsors millions of dollars. ERT's ePRO solutions enable clients to capture sensitive findings directly from their patients, a process that is critical to proving the efficacy of their compound and its effects on patient safety. ERT offers a quick and easy, phone-based, voice-response solution, which is designed and optimized to help its clients collect clinically valid and sensitive data directly from participating patients.
John Blakeley, Executive Vice President of ERT, comments, "We are pleased to be able to offer these informative papers to the scientific community as part of the new ERT Knowledge Series. We intend to expand upon these in the future, adding more innovative papers to the series on hot industry topics and sharing our expert knowledge on products and services for clinical trials."
Jeffrey Litwin's paper on ECG centralization examines how central core laboratories are playing an increasingly important role in cardiac safety during clinical trials. In recent years, cardiac safety concerns have been cited as the most frequent reason for many new drugs and compounds being withdrawn from the market or receiving a refusal of regulatory approval. This paper demonstrates the importance of rigorous and accurate ECG data collection and analysis during clinical trials, discussing the benefits of a centralized approach to ECG collection.
A second paper, entitled, "Is Centralization the Future for Cardiac Safety in Clinical Trials?", authored by Amy Furlong, looks at the importance of accurate and reliable ECG data collection and analysis. This paper expands on Jeffrey Litwin's paper to look at the future of cardiac safety in clinical trials. It covers the difficulty of estimating the true costs of cardiac safety, arguing the improved accuracy of digitally generated ECG data makes the centralized approach a more cost-effective option by reducing the need for retesting. It also discusses the need for innovative new instruments and the benefits gained by the introduction of highly compact ECG systems.
The third paper in the series, written by Michael Federico, investigates the increased risk of suicidal behaviors in patients as a result of medications. The paper examines how ePRO plays an increasingly important role in suicidality monitoring in clinical trials. It contrasts traditional face-to-face and paper-based methods of suicidality monitoring with electronic initiatives.
As part of ERT's new Knowledge Series, a complimentary webinar entitled Cardiac Safety: Best Science, Best Value will be held on Wednesday, 3 February, at 10:00 AM EST (3:00 PM GMT) and Thursday, 4 February, at 2:00 PM EST (7:00 PM GMT). This webinar will discuss the paradigm shift taking place in the balance between science and cost in the area of cardiac safety. This webinar aims to demonstrate this new shift providing sponsors with better science while at the same time helping sponsors to maintain or even reduce costs. For additional information and to register for either of these dates, please visit www.ERT.com
For further information on ERT and its technology and services, please email info@ERT.com, call +1 215 972 0420 or visit www.ERT.com.
For further press information, please contact Fiona Robinson, The Scott Partnership, 1 Whiteside, Station Road, Holmes Chapel, Cheshire CW4 8AA, United Kingdom. Phone +44 1477 539539, Fax +44 1477 539540, Email email@example.com
Based in Philadelphia, PA ERT (eResearchTechnology, Inc.) (www.ERT.com) is a global provider of technology and services to the biopharmaceutical, medical device, and related industries. The Company is the market leader in providing centralized core-diagnostic electrocardiographic (ECG) technology and services to evaluate cardiac safety in clinical development. The Company also provides technology and services to streamline the clinical trials process by enabling its customers to automate the collection, analysis, and distribution of clinical data in all phases of clinical development.
Statements included in this release may constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements involve a number of risks and uncertainties, which could cause actual results to differ materially from those expressed or implied from such statements. These risks and uncertainties include, without limitation, the Company's ability to obtain new contracts, variability in size, scope, and duration of projects, integration of acquisitions, competitive factors, technological development, market demand, and other factors described in the Company's filings with the Securities and Exchange Commission. The Company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events, or otherwise.
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