2019 Exhibitor Information

 

2019 Premier Exhibitors

23andMe is the leading consumer genetics and research company and the only such company with FDA-authorized health reports. Our mission is to help people access, understand and benefit from the human genome. 23andMe is now working with sites to empower customers to access to innovative therapeutic options through clinical trials.

An SCRS Global Impact Partner™
Advarra is the premier provider of IRB, IBC, and global research compliance services to clinical trial sponsors, CROs, hospital systems, academic medical centers, and investigators. We offer unmatched regulatory expertise and innovative technology to ensure the highest standards of research review are met, while putting participants first and meeting complex human research protection oversight requirements. Advarra supports all phases of research across multiple therapeutic areas to help make research altogether better.

BioClinica

An SCRS Global Impact Partner
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. bms.com

An SCRS Global Impact Partner™
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 products that together streamline research operations. Complementing Clinical Conductor in the suite are two new products. CCPay offers sites the ability to control finances and improve patient satisfaction with real-time payment reimbursements, using secure pre-paid patient payment cards fully integrated with Clinical Conductor CTMS. While CCText, the only fully CTMS-integrated, conversational 2-way text messaging site solution, has demonstrated results showing increased patient recruitment, engagement and retention.

An SCRS Global Impact Partner™
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. http://clincierge.com/

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!

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.

An SCRS Global Impact Partner™
Cognizant partners with biopharmaceutical and med-tech companies to develop strategies and apply solutions to healthcare challenges across the value chain. Our platforms and services are digitizing interactions between sponsors, investigators, patients, and regulators across every phase, helping the industry subtract time from clinical development and add it to patient lives. To learn more, visit Cognizant.com

An SCRS Global Impact Partner™Complion is a flexible, enterprise-wide platform that enables clinical research sites to centralize and process regulatory documents across their organization. Built by clinical researchers for clinical researchers, Complion removes walls between physicians, administrators and staff by intelligently providing secure access to the right document when they need it. Leading sites, hospitals, academic medical centers, health systems and cancer centers around the country use Complion to save money, improve compliance, and streamline operations.

Devana Solutions is dedicated to providing revolutionary software that automates the tracking of clinical trial study leads, contacts and performance metrics allowing research sites to win more studies. Devana is the first cloud-based sales solution built exclusively for research sites by research professionals. www.devanasolutions.com

An SCRS Global Impact Partner™
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.
Website: http://www.globalcarect.com/

An SCRS Global Impact Partner™
Greenphire’s technology solutions take a patient-centric and site-centric approach to driving data integrity and data completeness for sponsor, CRO, and site clients. Greenphire’s patient payment and communication system, the ClinCard System, is designed to improve the clinical experience for patients and sites, drive positive patient behavior, and increase patient retention and compliance. The ClinCard System also significantly reduces site and study team administration associated with patient payments and communication, enabling coordinators and study managers to focus time on ensuring data cleanliness and completeness. For more information, please visit www.greenphire.com.

Hylant works with life science and clinical research firms to manage expected and unexpected risks. Whether your organization specializes in medical devices, clinical research, clinical trials, pharmaceuticals, biotechnology or product and technology development, your Hylant team has the deep knowledge to partner effectively with you on your business insurance and risk management program. With over eighty years in business, we tailor solutions to our clients’ needs, negotiate and advocate on their behalf and solve business challenges allowing our customers to focus more on their business than insurance. Visit Hylant.com to learn more about how our experts can help your business succeed.

ICON

ICON plc is a global provider of outsourced development solutions and services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programmes that support clinical development. With headquarters in Dublin, Ireland, ICON currently operates from 97 locations in 38 countries.

Interspond, LLC is a Trial Management Organization (TMO) established in 2003 that works with a network of exclusive and affiliated, multi-therapeutic sites across the country. As such we seek to identify study opportunities for the sites with which we work. Once identified, we query the sites, submit them for consideration for participation, facilitate the study start-up process, and negotiate the contract and budget. Recently, Interspond signed an agreement to provide exclusive business development services to a network of neurology/rheumatology/ophthalmology sites. As a result, Interspond has a hybrid model working with sites on an exclusive and non-exclusive (affiliated) basis. We take pride in the long standing established relationships we have with many sites and delight in our outstanding reputation in the industry.

An SCRS Global Impact Partner™
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 www.iqvia.com.

An SCRS Global Impact Partner™
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

Medidata

An SCRS Global Impact Partner™
Medidata is leading the digital transformation of life sciences, with the world's most-used platform for clinical development, commercial, and real-world data. Powered by artificial intelligence and delivered by industry experts, Medidata helps pharmaceutical, biotech, medical device companies, and academic researchers accelerate value, minimize risk and optimize outcomes. Medidata and its companies, Acorn AI and SHYFT, serve more than 1,300 customers and partners worldwide and empower more than 150,000 certified users every day to create hope for millions of patients. Discover the future of life sciences: www.medidata.com


Medix

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.

An SCRS Global Impact Partner™
Oracle Health Sciences breaks down barriers and opens new pathways to unify people and processes to bring new drugs to market faster. As a leader in Life Sciences technology, Oracle Health Sciences is trusted by 29 of the top 30 pharma, 10 of the top 10 biotech and 10 of the top 10 CROs for managing clinical trials and pharmacovigilance around the globe. www.oracle.com/lifesciences.

Pfizer

An SCRS Global Impact Partner™
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 healthcare products. Our global portfolio includes medicines and vaccines as well as many of the world’s best-known consumer healthcare products. We collaborate with healthcare 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

An SCRS Global Impact Partner™
PRA Health Sciences is one of the world's leading global contract research organizations (CRO), providing outsourced clinical development services to the biotechnology and pharmaceutical industries. At PRA, providing innovative solutions for our clients is what we do. Side-by-side with our clients, we strive to move drug discovery forward, helping them to develop life-saving and life-improving drugs. PRA has more than 11,000 employees working in 80+ countries providing comprehensive clinical development services across all phases. From full service clinical development to the pioneering Embedded Solutions™ model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace. PRA has worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 50+ such drugs. www.prahs.com

RealTime Software Solutions, LLC is a global industry leader of innovative technologies that are streamlining the way research gets done! Solutions include the RealTime-SOMS system for sites that packages CTMS, eDOCS, eSOURCE, TEXT and PAY into a seamless system for complete site operations management at the single-site or enterprise level. RealTime is also bringing disruptive new technologies to Sponsors and CROs to further enhance the study management process. Learn more about RealTime solutions at www.realtime-ctms.com or call (210) 852-4310.

An SCRS Global Impact Partner™
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

An SCRS Global Impact Partner™
StudyKIK is the leading 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).

StudyTeam is the world’s most friendly patient recruitment platform where sites can discover, organize, and pre-screen the patients they need to reach their full potential. Learn more and sign up for free at StudyTeamApp.com

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.

An SCRS Circle of Innovation™ Partner
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.

An SCRS Global Impact Partner™
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.

An SCRS Global Impact Partner™
Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to streamlining the end-to-end clinical trial process, Veeva offers the industry’s first cloud platform that combines EDC, CTMS, eTMF, and study start-up to unify clinical data management and clinical operations. Veeva has more than 625 customers, ranging from the world's largest pharmaceutical companies to emerging biotechs.

An SCRS Global Impact Partner™
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.

VitaLink Research is wholly owned and dedicated solely to clinical research networks that connects researchers, doctors, and patients with the shared goal of bettering research across the industry - all in one place. We are a true “one stop shop” for high quality research and results. Each of our research facilities focuses solely on conducting clinical trials and collecting the most accurate data possible. Research should never be an afterthought. At VitaLink, it’s the priority.

WCG

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.

2019 Performance Exhibitors

abbvie

An SCRS Global Impact Partner™
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. Visit us at www.abbvie.com .

ACRP

ACRP makes your people better so your business can soar. Having the best people gives you the best of both worlds: lower costs and risk, and higher quality, efficiency, and certainty. That’s why gold standard talent leads to gold standard progress – to the next stage, next trial, or next product launch – helping your business change the world for the better. Learn more about how we help your business at acrpnet.org.

The Alliance for Multispecialty Research, LLC is a nationwide company of 17 Clinical Research locations recognized as among the most experienced in the industry. AMR acknowledges the importance of multi-site coordination using our standardized processes. This allows us to maximize economies of scale and consistency in order to exceed Sponsor goals ahead of schedule and under budget.

Antidote powers clinical trial search on hundreds of patient advocacy websites, including JDRF, Lung Cancer Alliance, Healthline, and many more. This search allows millions of patients to opt into trial notifications. Now, research sites can access this active network of engaged patients, and reach out to those whose profiles align with the eligibility criteria of a particular study.

Start connecting with patients in your area. Visit www.antidote.me.



An SCRS Global Impact Partner™
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

Barrington James are a Global specialist recruitment consul­tancy with offices in the USA, Europe and Asia Pacific that work across the Healthcare sector. Our structure, with separate divisions and dedicated consultants for the markets we serve ensures a thorough, professional and intelligent approach in both permanent and interim solutions. barringtonjames.com/

An SCRS Global Impact Partner™
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

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.

An SCRS Global Impact Partner™
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. Visit us at www.boehringer-ingelheim.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. www.brany.com.

Fully automated clinical trials and site management solution. Electronic source, drug accountability, and more. Created by experienced PI and proven in 300 clinical trials, 8 successful FDA inspections, and 11,000 patients. Intuitive Cloud application accessible from everywhere and on any device. Transform your site to paperless painlessly and reap huge benefits from this complete system that manages your trials from set-up to archive. Extensive demo's will be available. In the meantime, you can call 210.614.4800 for a demo and information!

ClinasystNG is a site-centric CTMS that offers an easy to use interface that will increase your site's efficiency in recruiting, scheduling, financial tracking and collections, team collaboration, and more. ClinasystNG is accessible from anywhere, touts advanced security features, and is priced with a small-site budget in mind. Redesigned in early 2017, Clinasyst has been increasing productivity for over 20 years. Visit clinasyst.net to request a demo and find out why more and more sites are choosing ClinasystNG!

ClinConsent is an innovative, regulatory-compliant, patient-friendly, electronic consent system (eConsent) powered by artificial intelligence for clinical trials. ClinConsent automates the patient enrollment process and onboard patients directly into any standard EDC, improving overall consent tracking management, reducing informed consent errors, and easing the administrative burden for sites and study teams. It also enhances the patient experience with easy-to-understand clinical trial information while improving participant compliance and boosting patient engagement. Visit us at www.clinconsent.com.

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.

Clinical Research Billing is a service for clinical research sites. We work with Clinical Conductor or RealTime to invoice, follow-up and reconcile payments. We take billing off-site, provide financial reports, and support site management, while our expertise in the CTMS makes it easier to use and increases cash flow. Our goal is to provide our financial experience to independent research sites so they can grow profitably and do more research. clinicalresearchbilling.com/.

Are you looking for a better way to hire quality research staff for your site? Clinical Research Fastrack pays sites to host exceptionally trained, passionate research professionals as interns. If you like your intern or any of our candidates, hire them at no cost. Visit us at http://clinicalresearchfastrack.com.

Compumedics offers comprehensive and innovative solutions. The latest ProFusion Sleep software, ProFusion Sleep 4, continues to be the choice platform for recording, analysis and reporting sleep studies. Compumedics’ new ProFusion NeXus 360 provides workflow efficiencies from the Cloud via a full web-based interface accessed from your PC or wireless device.


Elias Research Associates (SMO) works as a site advocate to effectively partner research sites with CROs and Sponsors. Elias provides professional administrative and financial services by centralizing weekly study opportunities at no upfront cost, streamlining document submission and communications, accelerating study start-up, and providing extensive contract and budget negotiation expertise.

Exostar enables thousands of companies within our connected Life Sciences community to work together via a single industry-trusted identity credential. Through streamlining research and development, Exostar speeds clinical trial management and overall time-to-market, while decreasing operating costs.

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.

Gen1

As a full-scale clinical research service company, Gen1 Research handles all aspects of the clinical trial process for a truly turnkey experience. Our extensive, multi-specialty network of research-ready physicians and patients allows us to match your study with the right participants across multiple sites.

GlaxoSmithKline

An SCRS Global Impact Partner™
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

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..

ImageBloom Logo

ImageBloom is a full service advertising agency that specializes in helping sites and sponsors improve their enrollment capabilities for clinical studies of all kinds. There is no one-size-fits-all approach, so our professionals with years of research experience will develop a plan for success on a local or global level.

Insearch

Insearch is a clinical business development company dedicated to study identification and the site selection process. Our exclusive network of principal investigators provides sponsors and CROs with experienced and successful clinical research sites located throughout the US. The network consists of more than 350 investigators at more than 250 site locations. The size of our network grants us a unique perspective into understanding the capabilities of each investigator and site, allowing us to match sponsor/CRO studies with sites that have the most appropriate combination of: investigator and staff experience, facility accommodations and access to qualified, committed research subjects. If you are a site that needs personal and productive business development or a sponsor/CRO that needs investigators that fit your studies, please come visit our booth. We are also available via our website www.insearchgroup.netcontact with Susanna Keilman (727) 544-4842, info@insearchgroup.net.

We improve people’s health experiences through creativity. Our global Clinical Trial Experience discipline combines patient, protocol, disease and media insights with data and technology, to deliver recruitment and retention solutions that provide measurable results – like 350,000 patients across 450 studies in 75 countries, and counting. langland.nyc/.

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.

Life Line Screening is the largest direct-to-consumer preventive health screening company in the U.S.; founded in 1993. They provide screening and close contact interaction with 700,000 patients at 15,000 events every year. Life Line has supported screening for over 60 clinical trials to date, delivering dramatic reductions to study timelines.

An SCRS Global Impact Partner™
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

MedPoint Digital

MedPoint Digital develops specialty eClinical platforms for investigator portals, virtual investigator meetings and monitor remote site visits. Our digital solutions enable sites to be more productive, with study eBinders, site message centers, eClinical sign-on centers, online study training and site dashboards. All systems are ICH-GCP compliant and designed to be user-friendly.

PAREXEL

An SCRS Global Impact Partner™
Parexel is focused on supporting the development of innovative new therapies to improve patient health. We do this through a suite of services that help life science and biopharmaceutical customers across the globe transform scientific discoveries into new treatments for patients. From clinical trials to regulatory and consulting services to commercial and market access, our therapeutic, technical and functional ability is underpinned by a deep conviction in what we do. For more information, visit our website and follow us on LinkedIn and Twitter. Parexel is a registered trademark of Parexel International Corporation. All other trademarks are the property of their respective owners.

PatientTrials

PatienTrials, a patient-centric platform, optimizing efficiency in patient recruitment and retention in clinical trials, is built for CRO’s, Sponsor and sites to monitor multiple studies, reduces risk and costs in running a clinical trial. With access to 250M patient records at 1000 hospitals and health systems, it creates an innovative way to embed health education into daily lives of people putting EMR information at their fingertips. PatienTrials promotes “Clinical Research as a Care Option”, connecting patients with clinical trials as part of their healthcare continuum.

PrepaidTechnology

Prepaid Technologies helps clinical research sites make their patient payments processes more seamless and cost-effective. Leveraging our 20-year history and diverse experience in the prepaid card space, combined with our ability to integrate with CTMS platforms and workflow processes, we deliver solutions that help improve retention and the overall patient reimbursement experience. Visit us at www.in-prepaid.com/scrs.

An SCRS Global Impact Partner™
Roche focuses on finding new medicines and diagnostics that help patients live longer, better lives and evolve the practice of medicine. Our company has a 120-year history of advancing the field of medicine and bringing novel treatments and diagnostics to patients. Our purpose is: Doing now what patients need next.

Introducing, Scout Clinical, a part of the Meeting Protocol Worldwide family. At Scout Clinical, we, provide a full range of patient concierge services on a global scale, having worked in 101 countries to date. These services include expense/reimbursement via debit card or electronic funds transfer, ground transportation, flights/trains, hotels, long-term housing, translation services, visa management, cultural liaison services and any special assistance required. At Scout Clinical we tailor each service to fit the unique needs of each study and sponsor. Reporting is customized to sponsor specifications providing useful, transparent and real-time data. We consult with the study team on the regulatory process for patient services, specifically related to ICF language and IRB/EC submissions. Our HIPAA and GDPR- compliant system is simple for patients, caregivers and site personnel to use. With over 22 years of experience organizing clinical travel and expense management, we understand clinical trials and the sensitivity required to provide patient services. Please visit our booth to learn more about Scout Clinical.

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.

SIGAL SMS are a Site Management Organization (SMO), which specializes in supporting the establishment and optimization of established physicians and outpatient practices, nationwide in Germany, on their way to become a professional study site. Our ambitious target is to become the largest and most successful network of study sites in Germany and to expand internationally.

The requirements on the route to the establishment and professionalization of a study site are individual, as is our support to you. SIGAL SMS stands for a dedicated and solution-oriented team, which assists you with a high level of expertise.n.com/" target="blank">www.janssen.com

Splash Clinical is an innovative patient recruitment firm that’s pioneered the use of digital & social media to recruit patients for clinical trials. The company was founded to help solve the problem of patient enrollment in clinical trials by leveraging the power of social media, data analytics and mobile technologies. Our team works with Sponsor’s and CRO’s from across the globe, supporting 5,000+ study sites in 19 countries. Over the past 7 years, Splash Clinical has proven successful completions of more than 300 digital & social media patient recruitment campaigns. Splash Clinical has a broad range of therapeutic experience including CNS, immunology, women’s health, oncology and rare & orphan disease states. With our extensive digital & social media knowledge, our campaigns reduce the time and diminish the expenses that are often required to recruit patients.

The Patient Recruiting Agency (TM) (TPRA) is a full service patient recruiting and retention organization supporting Sponsors, CROs, SMOs and Investigators in Canada and the United States since 1999. TPRA has been incorporated in Canada since 2004 and began recruiting patients in 1999. Since that time, TPRA has completed over 2,200 clinical trial campaigns for over 150 indications. Services include study branding, traditional and online media production and placement, study-specific websites, patient phone screening and RADIUS365TM, TPRA's online platform for tracking and managing all response, referral, randomization and retention activities in real-time. One of TPRA's specialties is the production and placement of customized direct-to-patient advertising and technological solutions specifically for clinical trials. The unique characteristic that sets TPRA apart from other competitors is that all services are performed by TPRA's own IN-HOUSE staff with no outsourcing which offers its clients greater flexibility, accountability and cost-efficiencies than those offered by other competitors. For more information about TPRA services and capabilities please contact Corrie Palm, or visit TPRA’s website, www.PatientRecruiting.com.

The PharmaSeek Companies are dedicated to helping sites improve the management of their research operations. Our seasoned professionals provide turn-key business solutions, which allow site personnel more time to focus on clinical activities. These outsource business solutions include Patient Recruitment, Medicare Coverage Analysis, Receivables Management, Short-term Study Financing, Budget Negotiation, and Contract Negotiation. To find out more about our services, please contact Ted Fuertges at (608) 664-9000 ext. 2231 or visit our website at www.pharmaseekcompanies.com.

PilotPay serves the Pharmaceutical, Biotech and Medical Device industries by providing stipend management, expense reimbursement, and travel solutions to study participants, globally. PilotPay Clinical reduces the administrative burden of sites, provides prompt, accurate payments to study participants, and provides sponsors with executive reporting at the ‘click-of-a-button’.

For over 28 years, Sterling IRB has been committed to protecting research subjects who play such a vital role in the development of new medicines and medical technologies. Sterling is fully accredited by AAHRPP, convenes daily board meetings, and has jurisdiction in the United States and Canada. www.sterlingirb.com

An SCRS Global Impact Partner™
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.

Founded in 2013, Trial Connections locates clinical trial opportunities for investigator sites across all therapeutic areas and phases. We offer cost effective business development services to help sites build their pipeline of study opportunities and grow their business. www.trialconnections.com

Founded in 2015 Teckro provides solutions to simplify and modernize clinical research for leading pharmaceutical and emerging biotech companies. To date, Teckro manages more than 100 clinical trials and is used by more than 11,800 active study sites around the world. Teckro employs more than 100 staff across its global headquarters in Limerick, Ireland, engineering excellence hub in Dublin, Ireland and its US-based office in Nashville, Tennessee. Visit www.teckro.com for more information.

An SCRS Global Impact Partner™
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.

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.

M3 Wake Research Integrated Site Network is an owned group of premier clinical research sites that is a unique and innovative resource for Phase I - IV clinical trials. We offer Principal Investigators with a wide variety of therapeutic expertise who conduct studies that are suitable for a demographically and geographically diverse pool of qualified individuals.

The Wake Research sites encompass 11 locations in 6 states across the Western, Southern and Southeastern United States with a database reaching nearly one million subjects. We offer partners centralized contract and regulatory support, and feature an in-house marketing and advertising team focused on quick-starts to enrollment.
 
Our board-certified physicians have completed more than 6,000 successful clinical trials. Clinical trials at our sites are completed on time and with accuracy.  We consistently exceed sponsor expectations for integrity, subject enrollment, human protection and expeditious delivery of accurate evaluable data.

XpertDox

XpertDox is a healthcare data analytics company dedicated to improving patient access to healthcare and clinical trials, especially for patients with rare diseases, by leveraging our comprehensive database of over 1 million U.S. doctors, 7,000+ diseases and 24,000 clinical trials.

  

2019 Site Solutions Summit Media Partners

PharmaVOICE magazine provides commentary about the challenges and trends impacting the life-sciences industry, covering a range of issues from molecule through market. PharmaVOICE's more than 41,000 BPA-qualified subscribers are also kept abreast of the latest trends through additional media resources, including WebSeminars, Podcasts, Videocasts, and White Papers.

2019 Alliance Sponsor

CSSi is a Site Performance Company. Our services focus on managing the clinical trial enrollment process and supporting sites to maximize their performance in meeting or exceeding patient accrual timelines. We work with each site individually to ensure that all efforts are specific to each site’s geography, staff availability, past experience and suggestions for the particular study. CSSi utilizes a highly talented in-house staff to deliver these services which allows us to meet your enrollment goals while being mindful of your study budget. We believe that setting each site up for success is best achieved by investing our efforts in developing site-specific enrollment strategies which minimizes costs and maximizes the sponsor’s return on investment. For more information regarding CSSi’s targeted enrollment services and capabilities please contact Chris Trizna, or visit the CSSi website, www.CSSienroll.com.

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