2018 Executive Sponsors
2018 Associate Sponsors
2018 Supporting Sponsors
2018 Exhibiting Companies
2018 Supporting Partners
2018 Media Partners
2018 Executive Sponsors
With nearly 50 years of clinical and therapeutic experience, ERT is a global data and technology company that minimizes uncertainty and risk in clinical trials so that its customers can move ahead with confidence. In 2017, ERT supported more than 60% of all FDA drug approvals. Learn more at www.ert.com.
goBalto is the industry leader in cloud-based study startup software for the global life sciences industry, offering the only complete end-to-end platform for starting clinical trials, from site identification, feasibility assessment and selection through to activation, with comprehensive metrics to track adherence to timelines and budget. For more information, visit www.gobalto.com.
2018 Associate Sponsors
EDETEK is an innovative clinical solutions company that provides high-quality technology and services to life sciences companies. Our digital clinical platform, CONFORM™, fulfills our clients’ data engineering and business analytics needs. Our metadata driven solution offers unparalleled advantages in data quality, time to completion, and cost efficiency. Visit www.EDETEK.com.
Elligo Health Research offers the only platform that brings clinical research to physician practices, accelerating the development of new pharmaceutical, biotechnology and medical device products and therapies. Our Goes Direct® approach uses state-of-the-art technology to compliantly leverage current electronic health record data and applies a proprietary, prescreening process to match protocol-eligible patients for participation in clinical studies. It is our mission to support health care providers by providing personnel, procedures, technology and infrastructure for clinical research, enabling patients to participate in research while remaining under the care of their own trusted physician. Learn more at elligodirect.com.
Forte provides software and services in the critical areas of clinical trial management, clinical data management and research administration for cancer centers, academic medical centers and health systems. With a strong belief in community, collaboration and standards-based development, Forte also facilitates the Onsemble Community, a customer-exclusive group for peer networking, best practices and support. Learn more at www.forteresearch.com.
GlobalCare Clinical Trials, LLC is the leading global provider of ambulant healthcare services for clinical trials. GlobalCare provides innovative, GCP-compliant services for biopharmaceutical companies by conducting selected study visits at locations convenient and comfortable for the patient when travel to the investigator site is not practical. GlobalCare’s traveling clinicians provide patients with a convenient way to participate in trials regardless of study duration, frequency of visits, their disease state or distance to the study site. Additionally, GlobalCare’s patient-centric approach helps to accelerate patient recruitment and improve study patient compliance and retention. Learn more about us at http://globalcarect.com.
Hawthorne Effect is a tech-enabled service that delivers timely, accurate and complete clinical trial data. Our network of HEROs, trained in clinical trial conduct and equipped with mobile technology, bring study visits to patients anywhere, anytime solving the problems of patient retention and missing data. Learn more at www.hawthorne-effect.
ICON plc is a global provider of drug development solutions and services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development – from compound selection to Phase I-IV clinical studies. With headquarters in Dublin, Ireland, ICON currently, operates from 84 locations in 38 countries and has approximately 12,300 employees. Further information is available at www.iconplc.com.
Medable is a user-friendly application platform purpose-built for healthcare and life sciences industries. Through our award-winning technology stack, we provide researchers the ability to connect, engage, and learn from patients and participants in real time, significantly reducing the cost and time it takes to get your clinical trial up and running. On Medable’s secure, HIPAA-compliant, “no coding required” platform, patient and provider-facing apps are easy to build and quick to deploy, enabling rapid enrollment, meaningful engagement, and actionable, real-world insights. Join us as we work with leading research teams to map the human digitome – providing the first digital signature of health and disease. Medable is transforming the way you work, treat, cure, and dream. For more information visit www.medable.com.
MedPoint Digital develops specialty eClinical platforms for clinical trial portals, interactive modules, virtual investigator meetings, and mobile patient apps. Our digital solutions enable sites, sponsors and CROs to be more productive, with online Training, Documents, eReg Binder™ (eISF), Alerts, Messages, SUSAR eSafe™, Site Tools, Visit Guides, InSite™ Virtual Monitoring, Single Sign-on and Metrics. For more information visit www.medpt.com.
MMG provides best-in-class global patient recruitment services. We have accelerated enrollment across all therapeutic areas, among specialty patient populations, and in more than 70 countries. Our expertise, commitment to excellence, and innovations have made us a trusted strategic partner to clinical study teams for three decades. Visit www.mmgct.com.
MRN specializes in the conduct of clinical trial visits in the patient’s home and supporting clinical trial sites with nursing resources. We understand the complexities of today’s clinical trial environment and the burden this places on both patients and sites. Our nursing services are designed to ease these burdens, accelerate patient recruitment and retention and maximise the impact of the trial for the sponsor. To learn more, visit www.themrn.co.uk.
Learn more at www.prahs.com.
Quotient Sciences is a CDMO:CRO pharma services business dedicated to accelerating drug development from first-in-human to proof-of-concept. Our formulation development, clinical pharmacology and clinical manufacturing services are provided either individually or as an integrated solution and our unique Translational Pharmaceutics® platform is proven to significantly shorten timelines and reduce development costs. Learn more about us at www.quotientsciences.com.
Saama Technologies is the advanced data and analytics company delivering actionable business insights for life sciences and the Global 2000. Saama is singularly focused on driving fast, flexible, impactful business outcomes for its clients through advanced data and analytics. Saama’s unique “hybrid” approach integrates focused solutions and expertise across the life sciences domain, business consulting, machine learning, automated data management, cloud and big data technologies. Saama’s approach integrates manual and disconnected data initiatives into a well-aligned roadmap facilitating the client’s journey from strategy through solution implementation. Learn more at www.saama.com.
Target Health Inc, a full-service CRO and clinical trials software company, serves the pharmaceutical, biotech, medical device and diagnostics industries with full regulatory and clinical trial services. In addition, Target Health has developed a full suite of software products supporting the paperless clinical trial. Our pledge is to optimize the life cycle of drugs, biologics and devices with expertise, leadership, innovation and teamwork. We provide superior, consistent performance with the highest standards of ethical conduct and integrity. For more information, visit www.targethealth.com.
WIRB-Copernicus Group (WCG) is the leading provider of solutions that increase efficiencies in the clinical trial process through innovation, clinical expertise, and technology. The industry’s first clinical services organization, WCG enables biopharmaceutical companies, CROs, and institutions to accelerate new treatments to patients, while maintaining the highest standards of human subject protections. Learn more at www.wcgclinical.com.
2018 Supporting Sponsors
Axiom, a recognized leader in the business of law, provides tech-enabled legal, contracts, and compliance solutions for large enterprises, serving 75% of the top-50 life sciences companies globally, including 9 of the top 10. The firm comprises 2,000-plus lawyers, professionals, process engineers and technologists who serve over half the Fortune 100 across 15 regions and 3 centers of excellence globally. Axiom’s solutions combine legal experience, technology, and data analytics to dramatically reduce risk and cost, including our clinical trial contracting solution to reduce negotiation time, accelerate drug development, and improve site satisfaction. Learn more at www.
2018 Exhibiting Companies
AiCure uses artificial intelligence (AI) to visually confirm medication ingestion on smartphones. The process is entirely automated. The clinically-validated platform reduces the risk of trial failure by increasing adherence, allowing for early detection of non-adherence, and ensuring optimal data quality. Trials benefit from increased statistical power and reduced costs. Learn more at www.aicure.com.
Through its products and technology-driven solutions, BBK Worldwide – newly rebranded as The Patient Experience Company™ – is committed to educating consumers, engaging participants, unburdening sites, and supporting sponsors, a combination essential for enhancing the clinical trial patient experience and advancing the industry’s R&D efforts. One of the few remaining corporately independent and full-service R&D marketing firms, BBK has maintained its position at the forefront of innovation for 35 years. Headquartered near Boston, BBK has partners and offices across Europe and the Asia-Pacific region. Learn more at www.bbkworldwide.com.
We offer a unique suite of solutions, with a unique perspective on clinical research development. We focus on bringing together best-in-class science, technology and service to drive superior clinical outcome results for our clients and for their patients. For more information, visit: www.bracketglobal.com.
CluePoints® is a Risk-Based Monitoring and Central Statistical Monitoring solution that has been designed and perfected over the last 15 years. It employs unique statistical algorithms to determine the quality, accuracy, and integrity of clinical trial data both during and after study conduct. Learn more at www.cluepoints.com.
Cmed is an innovative, full service, technology-led CRO, bringing together a team of experienced people and its own innovative technology to inspire and drive real progress throughout the clinical trial process. Cmed’s new generation Clinical Data Suite, encapsia®, streamlines the capture, management and reporting of clinical data beyond what is currently possible, offering live access to all clinical data and advanced insights, within a single platform. Learn more at www.cmedtechnology.com.
DataArt is a global technology consultancy that designs, develops and supports unique software solutions, helping clients take their businesses forward. Recognized for their deep domain expertise and superior technical talent, DataArt has earned the trust of some of the world’s leading brands and most discerning clients. Learn more about us at www.dataart.com.
Greenphire is the global leader in clinical trial payment automation. Greenphire is exclusively focused on optimizing clinical trial performance by streamlining payment processes from sponsors and CROs to sites and patients. The choice of industry leaders worldwide, Greenphire supports site centricity and sustainability, increases patient engagement and retention, and provides more comprehensive financial data, resulting in better trials. For more information, visit www.greenphire.com.
Built on the premise that the patient voice is critical to all phases of the product lifecycle, HealthiVibe offers a systematic, structured process for pharmaceutical manufacturers to engage with patients at every stage: from clinical trial design all the way through post-approval activities and research. Offering a full-service solution that spans a range of activities, from moderating patient advisory boards to fielding clinical trial participant surveys to performing qualitative and quantitative outcomes research, HealthiVibe works to help our clients continuously engage with patients, improve clinical trial design, and bring all aspects of the product lifecycle into alignment with patient needs. For more information, visit www.healthivibe.com.
snapIoT has created the industry’s first complete, self-service, mClinical Platform, snapClinical™ that covers the full scope of clinical trials including; eQualification, eConsent, EDC /ePRO /COA and reporting/ analytics. snapClinical creates, designs, launches and manages clinical trials without software coding and is validated for compliance with 21 CFR Part 11 and EU Annex 11. For more information visit, www.snapiot.com.
Trifecta is the global leader in investigator training. We’ve designed and developed training for hundreds of clinical trials worldwide. We’re raising the industry IQ with intelligent, easy-to-use live and online solutions that give you unprecedented control over the clinical training process. For more information, visit www.trifectaclinical.com.