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ERT Partners

 

At ERT, our goal is always the same — to deliver the most accurate and regulatory-compliant data that will empower our clients’ expert decisions. We proactively seek best-in-class partners who share our goal, because like us, they believe in driving client value and satisfaction. 

Best-in-Class Providers — Best-in-Class Partners

We establish strategic alliances and partner relationships with clinical pharmacology units, Contract Research Organizations (CROs) and ancillary service providers around the globe.

It is through these trusted relationships that we can recommend and coordinate all necessary resources for a comprehensive, cross-functional solution on any project, including Thorough QT/QTc Trials (TQT). We have experience collaborating with our partners — establishing harmonized project management and data integration to promote the speed, accuracy and efficiency of collecting, interpreting and distributing cardiac safety and clinical data.

 

Strategic Alliances

 

Covance: The ERT/Covance partnership establishes a platform for enhanced delivery of our cardiac services to our clients. At ERT, we have the expertise and capabilities to provide centralized ECG services powered by our robust and market-leading EXPERT Technology Platform, and we are proud to offer these same services to Covance’s clients. The breadth and depth of Covance’s clinical services — coupled with ERT’s commitment to innovative technology for the collection, interpretation and distribution of cardiac and clinical data — provides our clients with the comprehensive solutions vital to ensuring drug safety.


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Healthcare Technology Systems, Inc. (HTS) is the pioneer in developing clinical interactive voice response (IVR) systems to collect data directly from patients for pharmaceutical companies, healthcare organizations, and researchers. HTS also offers personalized IVR self-help programs for patients that work.

With academic origins at the University of Wisconsin and more than three decades of published research, HTS and its principals are world renowned for their research expertise, educational accomplishments, and innovative computer-administered rating scales.
 


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Integrium: Integrium is a cardiovascular- and metabolic-focused, full-service Clinical Research Organization (CRO) with an unrivaled reputation for conducting global clinical-development programs of the highest integrity. Pharmaceutical, biotechnology, diagnostic and medical device companies look to Integrium for a complete range of customized Phase I-IV programs and clinical-research services in cardiovascular and metabolic therapeutic areas that include biostatistics, data management, medical safety, quality assurance, regulatory affairs, medical writing services and cardiovascular core lab services, specializing in Ambulatory Blood Pressure Monitoring (ABPM) services. Combining its Integrium Clinical Excellence (ICE) operational methodology, its full range of clinical-research services and therapeutic expertise, Integrium leads sponsors to more confident, better-informed, drug- and device-development decisions. Integrium is headquartered in Tustin, Calif., with operational offices in Bedminster, N.J., and Johannesburg, South Africa.


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nSpire Health: nSpire Health develops and manufactures respiratory care products and provides related services in more than 100 countries. The company is focused on cardiopulmonary diagnostics, respiratory core lab services and disease-management solutions designed to improve health care productivity while increasing the overall quality of patient care. nSpire Health is the exclusive provider of PiKo® home health monitors and HDpft™ systems, the most accurate and precise pulmonary-function testing systems worldwide. ERT and nSpire have created an alliance to provide integrated cardiac safety and pulmonary core lab services to clinical researchers worldwide.


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ERT Partner Relationships

 

Applied Clinical Intelligence: Applied Clinical Intelligence provides decision makers with the trusted information they need to clearly communicate the value and safety of medical treatments, drugs and devices. Applied Clinical Intelligence enables pharmaceutical, biotechnology, medical device and health care customers to realize process efficiencies and resulting savings in cost and time.


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California Clinical Trials (CCT): Since 1983, California Clinical Trials (CCT) has been at the forefront of drug development. CCT’s best-in-class clinical experts, research staff and trained physicians all work together seamlessly to bring hope to patients around the world. Whether providing careful patient selection for Phase I studies, or experience in drug development and research for Phase II-IV operations, CCT quality and performance allow clients to make “go/no-go” decisions about your products.


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ChanTest: ChanTest works in partnership with customers to speed the drug-development process, save time and money, and ultimately, help make better, safer drugs. The preeminent ion channel services company, ChanTest serves its drug discovery and development customers with GLP (Good Laboratory Practice) safety assays and automated-profiling assays, using its library of ion channel-expressing cell lines.


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Charles River: For more than 60 years Charles River has been helping our global partners accelerate drug discovery and development by providing them with tailored research models and preclinical and clinical support services. Our offerings span the entire drug development process, from discovery through market approval, providing our clients a seamless partnership throughout.


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DecisionLine Clinical Research: DecisionLine Clinical Research, a CRO, provides early-stage development expertise to pharmaceutical and biotechnology companies. While experienced with many therapeutic areas, DecisionLine has significant domain expertise on measuring the drug effect of CNS (central nervous system) products.


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ICON Clinical Research, Inc.: ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. ICON specializes in the strategic development, management and analysis of programs that support clinical development — from compound selection to Phase I-IV clinical studies.


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PAREXEL: PAREXEL is a leading global biopharmaceutical services organization that helps clients expedite time-to-market through development and launch services. These include a broad range of clinical-development capabilities, integrated advanced technologies, regulatory-affairs consulting and commercialization services.


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PRACS Institute, Ltd.: PRACS is a full-service CRO that offers pre-clinical, clinical, bioanalytical and statistical research services to the pharmaceutical, biotechnology and skin care industries.


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Seaview Research, Inc. : SeaView Research provides Phase I and early Phase II clinical pharmacology testing to the pharmaceutical and biotech industries. SeaView prides itself in performing the most demanding and complex protocols while maintaining uncompromising standards of quality, integrity, and timeliness. We offer exceptional client-focused service led by a full-time staff of more than 160 employees including three board certified physicians, physicians assistant, a registered dietician, 2 pharmacists, and ACRP certified RN study coordinators. Our medical staff is highly experienced in the intricacies of thorough QT / QTc studies, having performed over 20 such studies in the past 5 years.
 


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Site Support Institute Co., Ltd. (SSI): Site Support Institute Co., Ltd. (SSI) is one of the leading nationwide SMOs (Site Management Organization) in Japan. SSI manages various duties derived from clinical trial implementation and assists medical institutions with performing various tasks throughout the clinical trial process.


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Statistical Resources, Inc.: Statistical Resources, Inc. is a strategic statistical, statistical programming and data-management resources consulting firm with special emphases and experience in the pharmaceutical, biotech and medical devices industries. Statistical Resources specializes in services specific to these industries for clinical studies and submission to the U.S. Food and Drug Administration (FDA) and other regulatory agencies worldwide.


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Swiss Pharma Contract, Ltd.: As an International CRO, Swiss Pharma Contract, Ltd. offers a variety of services focused on clinical pharmacology and clinical research, ranging from first testing of a new drug in man to post-marketing clinical studies.


www.pharmacontract.chback to top


 
 
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