Advarra is the premier provider of IRB, IBC and global research compliance services in North America. By combining the mutual strengths of Chesapeake IRB and Schulman IRB, Advarra delivers exceptional client service, innovative technology and unmatched regulatory expertise, providing integrated research compliance capabilities to help make research altogether better.
Bayer is a global enterprise with core competencies in the Life Science fields of health care and agriculture. Its products and services are designed to benefit people and improve their quality of life. At the same time, the Group aims to create value through innovation, growth and high earning power. Bayer is committed to the principles of sustainable development and to its social and ethical responsibilities as a corporate citizen. In 2016, the Group employed around 115,200 people. For more information, go to www.bayer.com.
Lilly is a global healthcare leader that unites caring with discovery to make life better for people around the world. We were founded more than a century ago by a man committed to creating high quality medicines that meet real needs, and today we remain true to that mission in all our work. Across the globe, Lilly employees work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to communities through philanthropy and volunteerism. To learn more about Lilly, please visit us at www.lilly.com and newsroom.lilly.com/social-channels.
Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible. For more information, please visit www.roche.com.
Syneos Health is the only fully integrated biopharmaceutical solutions organization. Our company, including a Contract Research Organization (CRO) and Contract Commercial Organization (CCO), is purpose-built to accelerate customer performance to address modern market realities. Created through the merger of two industry-leading companies – INC Research and inVentiv Health – we bring together more than 21,000 clinical and commercial minds with the ability to support customers in more than 110 countries. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. To learn more about how we are shortening the distance from lab to life visit SyneosHealth.com.
Bio-Optronics is the creator of Clinical Conductor, the leading CTMS for collaboratively managing multiple clinical trials and sites. Used by more research sites around the world than any other CTMS, Clinical Conductor is managing over 40,000 studies. Clinical Conductor is part of the CCTrialSuite, a comprehensive set of integrated, patient-centric clinical research management and eClinical products available from a single supplier that streamline research operations, ensure compliance and enhance research business growth. Adding to the power of Clinical Conductor in the suite are a growing set of new solutions, including Part 11 compliant CCeReg document management, CCeSource real-time data capture, mobile friendly CCeConsent, instant payment CCPay and 2-way texting CCText solutions that will have the most seamless CTMS integration in the industry. https://bio-optronics.com/
Bristol-Myers Squibb is a global BioPharma company firmly focused on its mission to discover, develop and deliver innovative medicines to patients with serious diseases. Around the world, our medicines help millions of people in their fight against such diseases as cancer, cardiovascular disease, hepatitis B and hepatitis C, HIV/AIDS and, rheumatoid arthritis. At Bristol-Myers Squibb, our BioPharma strategy uniquely combines the reach and resources of a major pharma company with the entrepreneurial spirit and agility of a successful biotech company. With this strategy, we focus on our customers’ needs, giving maximum priority to accelerating pipeline development. www.bms.com
Clincierge® improves clinical trial performance by reducing barriers to participation, enhancing enrollment, and minimizing drop-outs. Our expertise and services lessen burdens on patients, caregivers, and sites while improving communications and coordination. We help keep studies on schedule, on budget, and data quality high, while making patient concerns a priority. clincierge.com
As regulatory requirements expand and clinical trials grow more complex, it has become increasingly burdensome for research sites to manage documentation. Complion’s document and workflow management platform improves efficiency, compliance and transparency for research sites and sponsors.
Greenphire is the global leader in financial software for clinical trials. Greenphire’s best-in-class solutions optimize clinical trial performance by streamlining financial and logistical workflows from sponsors and CROs to sites and patients. Greenphire’s ClinCard and eClinicalGPS solutions easily handle any type of trial design and complexity, resulting in more accurate and compliant payments globally for both sites and patients. ConneX is the most personalized clinical trial travel solution designed specifically to meet the recruitment and retention goals of domestic and international clinical trials. The choice of industry leaders worldwide, Greenphire provides better performance and better data, resulting in better trials. www.greenphire.com.
At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety, and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world’s best-known consumer health care products. We collaborate with health care providers, governments, and local communities to support and expand access to reliable, affordable health care around the world. For more than 150 years, Pfizer has worked to make a difference for all who rely on us. pfizer.com
VirTrial has a stable, long-standing virtual care platform customized for clinical trial use with both patient and site needs in mind. VirTrial is transforming the use of telemedicine in the clinical research industry by offering a patient management program that combines video, text, and email for clinical trial sites to easily and conveniently address specific patient and/or study needs in a secure environment. The platform can be used on any device and at any site. The company vision is to replace 25-40 percent of standard clinical trial visits with virtual visits to create hybrid studies. This model is best suited for Phase III and IV studies, rare diseases and to replace traditional telephone calls within a protocol. VirTrial enables higher performance by clinical trial sites, greater accessibility to trials for patients, and improved outcomes for pharmaceutical companies. Working together we can bring better medications to market more quickly. https://www.VirTrial.com.
Virtual Pre-Site is a virtual solution to streamline and standardize the Pre-Site Study Visit (PSSV) process. The solution decreases time and costs associated with the clinical trial startup process and ensures consistent information for all sites. It includes delivery of smart glasses with a camera that enables the Clinical Research Coordinator (CRC) to show the Clinical Research Associate (CRA), who is performing the site qualification visit remotely, all the items on the PSSV checklist simply by walking through the site wearing the glasses. Everything in view of the study coordinator streams to the CRA’s computer screen so she/he can verify the site has the needed equipment and space to conduct the study. Virtual Pre-Site’s secure, HIPAA-compliant platform enables the CRA to conduct video interviews with both the CRC and the PI to ensure they have the needed patients, appropriate experience, and time to conduct the study. For more information about Virtual Pre-Site, visit www.virtualpresite.com.
WCG is the leading provider of knowledge-based solutions that measurably improve the ROI of clinical research. For over fifty years, WCG has protected the rights and well-being of clinical research participants, fueling progress by keeping volunteers safe. By protecting people, the company has gained unique insight into every aspect of clinical trial operations and collected independent, verifiable data from over ninety percent of the world’s trials. Today, WCG is using those insights to help our clients make better, more informed decisions about the conduct of their trials. Applied to a single research study–or even more effectively, across an entire research program–WCG’s data-driven solutions have been proven to accelerate timelines, reduce costs, and increase the safety of clinical research. By removing many of the operational barriers to success, WCG is helping to maximize the value of clinical research.
AbbVie is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the world’s most complex and critical conditions. The company’s mission is to use its expertise, dedicated people and unique approach to improve treatments and advance health solutions for people around the world. www.abbvie.com
Barrington James is a uniquely successful specialist life science recruitment company and has recently been recognized as a BEST COMPANY To Work For by the Sunday Times. It has enjoyed an exceptional growth trajectory since its launch in 2002, and is now established in the heartlands of the international pharma, medical devices and healthcare industry with consultant staff already approaching 140, and planned to be 180 by the end of 2018.
BRANY is a clinical trials service provider, offering an array of comprehensive and efficient support services to Sponsors/CROs, Institutions, Hospitals and Private Sites conducting research. Over the past 15 years, BRANY has worked diligently to develop a strong infrastructure of services that support researchers and organizations in their pursuit to conduct quality research. BRANY’s unique model offers Local/Central IRB, Study/Site Identification, Contract and Budget Negotiations, Clinical Trial Coverage Analysis, Research Education, Research Compliance and Consulting services.
ClinEdge and BTC Network provide a full range of clinical and outsourced business services to clinical research sites, pharmaceutical companies, and CROs. Together, the two companies represent four business segments: two global networks of research clinics with over 1,000 physician investigators, site financial management, and patient recruitment/retention. Recruitment and retention services include, but are not limited to, online engagement and advertising, a national patient database, patient travel concierge, national and local advocacy, and an in-house call center. With extensive experience across over 300 different medical indications representing all therapeutic areas, the ClinEdge and BTC Network teams have helped to successfully conduct thousands of clinical studies over the last several years. Come by and talk to one of our representatives to see what we have been up to! If you are too busy to see us you can also drop Christian Burns an email at Christian@clin-edge.com or visit www.clin-edge.com or www.btcsites.com. Don’t forget to come to SCRS’s best party on Friday night!
Elligo Health Research, a healthcare-enabling research organization, uses electronic health records and the trusted patient and physician relationship to ensure all patients have access to clinical research as care. Powered by our novel IntElligo Research Stack™ technology and Goes Direct® approach, we connect more physicians and their patients to research.
Florence advances clinical trials with through software for managing document and data flow between research sites and sponsors. Florence eBinders is trusted by 2,000+ research teams for eRegulatory/eSource management, and Florence eHub is revolutionizing site-sponsor connectivity in a shared workspace for startup, monitoring, and quality control.
GlaxoSmithKline – one of the world’s leading research-based pharmaceutical and healthcare companies – is committed to improving the quality of human life by enabling people to do more, feel better, and live longer. www.gsk.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. www.globalcarect.com
IntegReview IRB provides ethical review for oncology research studies in the U.S. and Canada. Daily meetings. Customer support 24/7 with 24-48 hour document turnaround. Consulting, translation and pre-review services. Online real-time document management. Quality-driven. Responsive, experienced and flexible while maintaining ethical integrity. Fully accredited AAHRPP. Woman-owned independent IRB since 1999.
Inteliquet brings a new level of precision through a large, real-world data set, advanced predictive analytics, and digitization of trials. Moving beyond traditional patient recruitment, this innovation connects the right trial, to the right sites, and to the right patients—and helps move clinical trials into clinical care.
Medix Clinical Research offers workforce solutions and consulting services for sites, sponsors and CROs. Our in-house clinical research expertise will help you enhance operational strategy, maximize financial efficiency and bolster your talent pipeline.
RealTime Software Solution is a global leader in SAAS-based Clinical Trials Management Systems for Sites, Sponsors, and CROs. RealTime is also the only CTMS vendor that can offer a complete suite of solutions into a seamless platform, SOMS (Site Operations Management System). SOMS includes the industry-leading CTMS, SitePAY, TEXT, eDOCS, and eSOURCE which is accessible through an easy-to-use MobileAPP. RealTime also has the most advanced multi-site and site network enterprise systems available anywhere.
Total Clinical Trial Management (TCTM), is a contract research organization based in Dallas, Texas. TCTM has a unique perspective on emphasizing the relationship with the clinical research site as a primary driver for successful clinical trial completion. TCTM has a wide range of therapeutic expertise with recent areas of focus including pain, orthopedic injury, GI, dermatology, cosmetics, over-the-counter (OTC) and generics studies.
Trifecta is a global leader & trusted partner with deep experience in clinical trial technology solutions for leading pharmaceutical, biotech and clinical research organizations. Trifecta offers clinical trial solutions including: Online/On-Demand Investigator Training, Live & Web-Based Investigator Meetings, Safety Letter Delivery and Document Exchange. To learn more, please visit www.trifectaclinical.com.
Veeva is the leading provider of clinical operations technology to more than 200 sponsors and leading research organizations. Veeva SiteVault Free is a 100% free eRegulatory / ISF system that reduces the administrative burden in clinical trials by simplifying the management of regulatory documents and processes across all studies. Learn more at booth #34 or at https://sites.veeva.com/.