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

Accellacare (Previously PMG Research & MeDiNova) is a global clinical research network increasing patient recruitment and retention with a patient centric approach.   Accellacare extends across 77 active research sites in six countries with expertise in a wide range of therapeutic areas.  It has relationships with 275 Principal Investigators connecting it to 8 million+ patients. https://www.accellacare.com/

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection, and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. www.astrazeneca.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/ 

Boehringer Ingelheim is committed to improving lives and providing valuable services and support to patients and their families. Our employees create and engage in programs that strengthen our communities. Since its founding in 1885, the company has remained family-owned and today creates value through innovation for three business areas including human pharmaceuticals, animal health and biopharmaceutical contract manufacturing. www.boehringer-ingelheim.com

An SCRS Global Impact Partner™ With more than 500,000 registered members, growing at an average of 6,000-10,000 new registrants per month, HealthCarePoint has become one of the fastest growing networks in healthcare and clinical research and is poised to save the industry (Sponsors, CROs, Investigator Sites, IRBs, and Regulatory Agencies among others) billions of dollars in time and resources.

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

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.

Clinical.ly provides differentiated technological solutions to the clinical research industry, helping research facilities focus on conducting studies as efficiently as possible. Clinical research sites operate in a highly-regulated, fast moving and constantly evolving environment, with many stakeholders. By leveraging technology to reduce or eliminate tedious manual labor, you can focus on your business and these important stakeholders.

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!

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.

Covance, the drug development business of Laboratory Corporation of America^® Holdings (LabCorp^®), is the world’s most comprehensive drug development company, dedicated to advancing healthcare and delivering Solutions Made Real^®. www.covance.com

Clinical Research IO (CRIO) is an e-source and site workflow solution for investigators. Customize source templates and use a tablet to capture data quickly and accurately. Our system is a revolutionary new way of performing clinical 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.

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.

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

hyperCORE International is a super network of highly experienced and awarded clinical research site organizations. An industry leader providing Phase I-IV clinical trial services with more than 85 sites globally. Its innovative and collaborative partnership model redefines the way Sponsors, CROs, and sites engage in delivering meaningful research to patients.

ICON is a global provider of outsourced drug development services to biopharma, medical device, government, biosimilar and generic organisations. We offer a full range of clinical, consulting and commercial services that range from trial design to full study execution, and from clinical to post-market commercialisation. Our services are supported by in-depth therapeutic and regulatory expertise and market-leading technology and analytics. We are the only full service CRO that offers the knowledge, software and systems for adaptive trials.

IQVIA (NYSE:IQV) is a leading global provider of information, innovative technology solutions and contract research services dedicated to using analytics and science to help healthcare stakeholders find better solutions for their patients. Solutions are powered by the IQVIA CORE™, which combines big data, advanced technology, analytics and extensive industry knowledge. Formed through the merger of IMS Health and Quintiles, IQVIA has approximately 55,000 employees worldwide. Learn more at iqvia.com.

At Janssen, we are dedicated to addressing some of the most important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Driven by our commitment to patients, we develop innovative products, services and healthcare solutions to help people throughout the world. Janssen-Cilag International NV is part of the Janssen Pharmaceutical Companies of Johnson & Johnson. www.janssen.com

Ledger Run’s mission is to optimize the “Clinical Trial Ecosystem” to streamline, secure, and enhance the interactions between sites, sponsors, CROs, and others involved in clinical trial operations. Driven by a unique combination of deep domain expertise and technical capabilities, our ClinRun platform rethinks trial administration through active engagement, smart design, and breakthrough technology. Join us in enabling sites to engage more effectively with sponsors and CROs to expedite negotiations and promote a sustainable research community.

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.

Medidata is the leading global provider of cloud-based solutions for clinical research in life sciences, transforming clinical development through its advanced applications and intelligent data analytics. The Medidata Clinical Cloud™ brings new levels of productivity and quality to the clinical testing of promising medical treatments, from study design and planning through execution, management and reporting. www.mdsol.com

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.

Medpace is a global full-service clinical research organization (CRO) providing Phase I-IV core development services for drug, biologic, and device programs. Medpace has strong experience supporting development programs across therapeutic areas including oncology, cardiovascular, metabolic/diabetes, infectious diseases and vaccines, neuroscience, regenerative medicine, gastrointestinal diseases, pediatrics, and orphan disease. From feasibility, research site compatibility, safety, and logistics, Medpace brings efficiencies and operational excellence to both drug and device development programs. www.medpace.com

Oracle Health Sciences is the market leader in clinical solutions delivering transformative value for R&D in a modular, integrated, secure and high-performing cloud environment. We enable trial sponsors and CROs to optimize trial efficiency while reducing cost and risk from startup through submission; collect, deliver, and analyze higher-quality data faster; and help ensure patient safety during clinical trials and post-marketing surveillance. www.oracle.com/healthsciences.

PAREXEL provides comprehensive drug development capabilities to help clients get their new and innovative drug treatments into the hands that need them most. We simplify the journey to market through our global regulatory expertise, Phase I-IV clinical research services, integrated eClinical technologies, and commercialization services. For more information, visit www.PAREXEL.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. www.pfizer.com

PRA Health Sciences delivers innovative drug development solutions that improve patients’ lives. Our people are passionate about clinical research, working tirelessly to provide quality results. We offer exceptional experience across all phases and therapeutic areas and a broad spectrum of solutions, ranging from full-service clinical development to a pioneering embedded model. With 16,000+ employees covering 90+ countries, we bolster an impressive global presence with keen local insights. Our project teams harness their understanding of local regulations, standards of care and cultural customs to effectively align our approaches with each study’s unique goals. At PRA, we love what do because we are making a difference in the lives of patients and their family members worldwide. Over the years, we have contributed to the development of numerous drugs now available to countless patients. From our scientific and medical experts to therapeutically aligned project managers and monitors, we provide the commitment and expertise needed for today’s complex study. www.prahs.com

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.

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.

Sanofi, a global healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients’ needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new Genzyme. Sanofi is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY). www.sanofi.us

SentralBinders is a new electronic source and Investigator Site File system that has the benefits of paper without the need for printing and storage. Collect data quickly and efficiently with a system that works the way you do. Mark it up, file it, have it viewable by all and then come back later to make necessary corrections. Have all of your study documents available to everyone at all times.

The speed, quality, and integrity of endpoint evidence is everything in being able to efficiently advance an experimental therapy forward. Signant is the evidence generation company that helps you digitally enable trials. No matter how or where you run your trials. We make the patient journey more natural and intuitive, and the data journey more direct and objective. With our SmartSignals ecosystem, Signant delivers proof at the speed of life, simplifying and streamlining data generation and reducing the reliance on paper-based evidence gathering and management. We offer vision at a time of change as well as reliability and dependability where it matters most. When the world is counting on you, count on Signant.

Website connecting patients to clinical trials through thousands of social media communities across Instagram, Snapchat, Facebook, Twitter, and Pinterest. Live in 24 hours, sites receive 30-200* patients every 30 days. Sites can maximize enrollment with Tools including: StudyKIK Patient Messaging Suite (Instant Text Messaging, Appointment Reminders, & Text Blasting).

SubjectWell is the first risk-free clinical trials marketplace for patient recruitment. SubjectWell accelerates enrollment by engaging the 96% of Americans who have never participated in a clinical trial. And trial sites only pay for patients who randomize.

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.

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.

TrialScout™ provides high-quality Clinical Research Sites with a powerful new patient engagement and retention platform that builds their brand with patients and sponsors. TrialScout supports your clinical trials with its first-ever patient experience ratings and reviews, generating unique monthly analytics to optimize your Site operations. TrialScout helps patients find your clinical trials and supports them in choosing your Site, while keeping them engaged to reduce dropout. For more information visit www.TrialScout.com.

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 https://sites.veeva.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.

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.