2018 Exhibitor Information

 

2018 Premier Exhibitors

Acurian

An SCRS Global Impact Partner
Acurian is a leading full-service provider of clinical trial patient enrollment and retention solutions for the life sciences industry. The company increases the enrollment performance of investigator sites worldwide by identifying, contacting, prescreening, and referring people who live in the local community but are unknown to a research site. As a result, trial sponsors complete enrollment without incurring the unexpected expense of adding sites, time, or CRO change orders. Acurian’s investors include Euclid SR Partners, ProQuest Investments, JP Morgan Partners, Flatiron Partners, CDP Capital Technology Ventures, and Merck Capital Ventures. www.acurian.com

BioClinica

An SCRS Global Impact Partner
Bioclinica is a specialty services provider that utilizes expertise and technology to create clarity in the clinical trial process so sponsors can see key details, uncover hidden insights, and make better decisions. Bioclinica is organized by three business segments and serves more than 400 pharmaceutical, biotechnology and device organizations – including all of the top 20 – through a network of offices in the U.S., Europe and Asia. Representatives from  Financial Lifecycle SolutionsResearch Network and Patient Recruitment-Retention divisions will be available to meet, review your requirements and discuss opportunities to partner.

An SCRS Global Impact Partner™
Clinical Conductor is the industry’s first collaborative and configurable CTMS for managing research or executing clinical trials. The system provides users with the specific features and functionality they need to recruit effectively, improve overall patient visit satisfaction, maintain billing and research compliance and maximize profitability. Used by over 1,800 organizations around the world, Clinical Conductor provides organizations with the tools they need to raise the bar in clinical research.
www.bio-optronics.com

HealthCarePoint

An SCRS Global Impact Partner™
With more than 1,500,000 registered healthcare professionals worldwide, growing at an average of 15,000 – 22,500 new registrants per month, BlueCloud® has the fastest growing networks in healthcare and clinical research. A global networking technology that enables industry stakeholders to create new and efficient business models that improve patient care by implementing standards and eliminating waste and fraud. This ecosystem allows the exchange of “real-time” information required by regulatory agencies. BlueCloud acts as the catalyst for standardizing global programs like the NIH Stroke Scale (NIHSS), Modified Rankin mRS, Barthel Index (BI), Suicidality Scale (C-SSRS) and other diagnostic neuroscience programs. Let’s save lives, together!”.

For more information visit www.healthcarepoint.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.

At Clinical Trials of South Carolina, our mission is to safely advance science and improve lives through quality-driven research, collaboration and innovation. Our team of dedicated recruiters, coordinators and research assistants lead us to conduct top-level research studies across multiple therapeutic areas.

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

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.

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.

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

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™
goBalto develops next-generation solutions that simplify and accelerate clinical study startup in the pharmaceutical, biotechnology, and medical device industries. We have partnered with more than half of the top 20 pharma and 5 of the top 10 CROs in study startup, including: Novartis, Genentech Roche, ICON, INC Research, and Covance. Visit us at www.gobalto.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

An SCRS Global Impact Partner™
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.

Medidata

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

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.

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.PRAXEL.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

Quorum Review IRB is a privately-held, independent ethics review board fully accredited by AAHRPP. Our mission is to safeguard the rights and well-being of research participants. With 15 board meetings a week, we provide sponsors, CROs, institutions and sites with reliable, responsive service to support efficient study start-up and management.

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.

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).

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.

Synexus is the world’s leading SMO and operates a network of 27 dedicated research and 68 affiliated sites. All Synexus sites are fully staffed by GCP trained investigators, supported by patient engagement, project management and medical teams. Synexus is dedicated to trial excellence across cardiovascular, metabolic, musculoskeletal, respiratory and CNS diseases.

TrialScout transforms the experience of finding and participating in clinical trials for patients everywhere.

Sites, sponsors and CROs leverage TrialScout to more efficiently and effectively share their story and engage patients to consider participating in their trials.

With objective, independent ratings informed directly by patient reviews, TrialScout empowers prospective new patients to confidently select a trial site trusted by their peers.

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.

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.

2018 Performance Exhibitors

ACRP

The Association of Clinical Research Professionals (ACRP) is setting standards for clinical research competence and workforce development. A Washington, DC-based non-profit organization with more than 13,000 members, ACRP supports professionals and organizations across the clinical research enterprise with the Membership, Training, and Certification programs necessary for clinical trial quality and efficiency improvements.

Advarra is the premier provider of IRB, IBC and global research quality and compliance consulting services in North America. We provide customized, dedicated services for more than 2000 institutions, academic medical centers and research consortia and are fully sIRB ready. By delivering exceptional client service, innovative technology and unmatched regulatory expertise, Advarra provides integrated research compliance capabilities to help make research altogether better.

Our people are everything. Since 1983, Aerotek has become a leader in recruiting and staffing services by building quality relationships that allow us to place quality people in quality jobs. With over 250 non-franchised offices, Aerotek serves 18,000 clients and 300,000 contract employees every year. To learn more, visit Aerotek.com.

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.

Founded in 2009, Alpha Clinical Systems (ACS) is the leading provider of affordable and comprehensive next-generation eSource solutions. Developers of ACS360, a fully-integrated, cloud-based platform that provides direct eSource data capture with or without existing EDC systems, ACS streamlines clinical research by capturing data the moment it’s generated. Working with sites, sponsors and CROs, ACS helps customers maximize clinical trial efficiency and data quality while minimizing burden. From recruitment and scheduling to budgeting and forecasting, our fully-integrated platform streamlines workflows and eases eSource adoption. Discover the next generation of eSource at www.alphaclinicalsystems.com.

We are a dedicated clinical research site in NJ whose mission is to enhance longevity and quality of life through clinical research investigating new cutting-edge medicines. Associated with family and GI practices having over 130,000 active patients, we employ a patient-centric model leveraging lean and six sigma methods resulting in low protocol deviation rates, rapid enrollment, high retention, same-day data entry and query resolution.

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/

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!

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.

An SCRS Global Impact Partner™
Clinical Ink is an innovation-driven eSource solutions company dedicated to delivering technology that makes clinical research easier for sites, sponsors, subjects and regulators. Developers of SureSource, the first purpose-built electronic source record (ESR) that provides cleaner data more quickly, Clinical Ink is dedicated to eliminating paper documentation in clinical research. For more information, please visit: www.clinicalink.com

CRF Health is the leading global provider of patient-centered eSource technology solutions for the life sciences industry. With experience in more than 800 clinical trials, over 100 languages and across 74 countries, the company delivers best in class, fully integrated eSource solutions for pharma partners. Solutions include TrialMax, an eCOA suite which consistently demonstrates the industry’s highest data accuracy, patient and site compliance, and patient retention, and TrialConsent, the patient-cenetred, intuitive and interactive informed eConsent suite. Learn More at www.crfhealth.com/


MCSP was established based on the needs and demands of clinical research site professionals across the country. We have a network of research sites who share centralized processes, training, contracts, and budgets. Our sites specialize in Respiratory Research, Sleep Medicine, Gastroenterology, Pediatrics, Internal Medicine, Endocrinology, Rheumatology, Allergy, and CNS. We have also developed preferred partnerships with Sponsors and CRO's. We are members of The Society for Clinical Research Sites (SCRS), because as sites we deserve to have a unified voice before our partners, regulators, and industry stakeholders.

DrugDev, a QuintilesIMS company, provides the pharmaceutical industry with DrugDev Spark, the only unified clinical operations suite comprised of proven solutions for study planning, startup, site payments, eConsent and trial management.
www.drugdev.org

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 eBinders is the solution for simplifying and advancing clinical research. Trusted by more than 3,000 sites around the world our only focus is equipping sites and sponsors with the best eRegulatory, eSource and contract management solutions.

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

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

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 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.net or direct contact with Vincent Napoli (727) 544-4842, vnapoli@insearchgroup.net.

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.

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.

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.

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.

Patient Advertising Guru is a niche provider of advertising and media buying services that exclusively serves the healthcare industry. We offer patient driven advertising expertise and access to our tremendous purchasing power, enabling us to pay far less for media. That’s why a broad range of healthcare providers, from private practices to hospitals will turn to Patient Advertising Guru to execute their advertising campaigns. In fact, many of the largest pharmaceutical manufacturers in the world have relied on our team to enroll research studies for the treatments you might be marketing today.

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

PharmaSeek Companies

Sister companies, PharmaSeek and PatientWise, are industry leaders in administrative services for clinical research. We partner with sponsors and CROs to identify sites for studies, facilitate rapid study start-up, conduct protocol cost savings analysis and implement central advertising campaigns. In addition, we provide administrative services to research sites. Our goal is to assist research organizations in achieving their objectives as efficiently and effectively as possible. To find out more about our services, please contact (608) 664-9000 or email us at info@pharmaseek.com.

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.

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.

Rocket Trials is a Patient Recruitment and Retention company specializing in clinical research trials. We help sites recruit patients both from within their own internal database, using our Rocket Referral App, and also outside patients by running targeted digital marketing campaigns. We then deliver all the leads inside our user-friendly portal.

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

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.

Slope.io: Clinical trials require a lot of drugs, kits, supplies, and equipment. Slope’s coordinator-centric solution for inventory management helps organize, track, and manage everything busy study sites use to move research their forward. Our “no surprises” approach ensures that sites are always prepared for every patient visit.

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.

SRI’s Clinical Trial Unit: Phase 1–3 expertise; 13-bed/three infusion-chair facility; 24-hour medical monitoring, onsite physician availability; high caliber physician network supported by professional staff, numerous therapeutic specialties; extensive patient databases; Neurology and Orthopedic Pain Management experience.

Backed by decades of experience in innovative solutions to meet clients’ needs. sri.com/biosciences

For more than 27 years, Sterling IRB has helped lead the way in safeguarding the rights and welfare of clinical research participants. Our approach places the focus on your specific needs – complete with caring, responsive service and a single-point-of-contact you can always count on. This means being there for you with the guidance and answers you need when you need them – all backed by a commitment to the highest standards of human subject protection and regulatory compliance. Sterling is fully accredited by AAHRPP, and has oversight capabilities in the U.S and Canada. www.sterlingirb.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.

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.

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

Virtrial is a technology company using a stable, long-standing telehealth platform to transform the clinical trial industry. The platform offers a patient management program that combines video, text, and email allowing pharmaceutical companies and CROs to create patient centric trials by replacing some study visits with virtual visits. The vision is for 25-50% of visits to be conducted virtually creating a hybrid model. This model is ideally suited for Phase III and Phase IV trials. Our post-approval patient management program allows sites to utilize efficient automated messaging. The Virtrial app is supported on any device (Android, Apple, iPad, Computer) and can be used by any site. It is hosted in a secure, cloud-based, environment and is HIPAA compliant. For more information please visit, www.virtrial.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.

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.

  

2018 Summit Experience Partners

 

Eagle Award Gala & SCRS Studio Sponsor

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.

 

Opening Reception & Table Talk Sponsor

RealTime-CTMS, the newest Clinical Trial Management System for investigative sites. Unlimited users, unlimited locations, unmatched user-friendliness and workflow management. We also offer website development and true website integration for study listings. If you are looking for a great new CTMS system or need to make a change, we can help. Please contact Rick Greenfield at (210) 386-4201 or visit our website at www.realtime-ctms.com

 

President's Reception Sponsor

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.

ACRO 

First-time Attendee Reception Sponsor

CSSi

Master Workshops 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.

HealthCarePoint 

Premier Networking Breakfast Sponsor

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. For more information visit www.healthcarepoint.com
 

Exclusive Networking Breaks Sponsor

Rocket Trials is a Patient Recruitment and Retention company specializing in clinical research trials. We help sites recruit patients both from within their own internal database, using our Rocket Referral App, and also outside patients by running targeted digital marketing campaigns. We then deliver all the leads inside our user-friendly portal.

Hylant 

Saturday Lunch Sponsor

Hylant Group’s Life Science Practice has expertise in tailoring insurance and risk management programs that respond to the changing exposures Life Science organizations face everyday. Hylant advises and consults with organizations in the Clinical Research, Medical Device, Pharmaceutical, and Clinical Trial industries. In this complex and ever changing environment, it’s important to trust an advisor who understands the industry and your business goals while delivering a program that reduces operating costs, improves efficiencies, while protecting assets and reputations. For more information please contact Michael Yon at 513-354-1612. www.hylant.com

StudyKIK 

Opening & Welcome Session Sponsor

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).

Medix 

Talent Development Sponsor

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.

Official Attendee Badge Holders Sponsor

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.

 

Official Attendee Bag Sponsor

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

 

Summit Portfolio Sponsor

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

2018 Summit Alliance Sponsors


Advantage Clinical is a full-service provider of eLearning and training in the clinical research space; providing sites, sponsors and CROs with the knowledge and skills to increase the quality and efficiency of their clinical research programs. Whether you are looking to train new employees, improve team performance, maximize patient recruitment or stay current on emerging topics, Advantage Clinical has a course for you. Advantage Clinical partners with clinical research sites and site networks to offer affordable training subscriptions to ensure your ever growing team is trained and ready to hit the ground running.


Clinical Research Billing works for independent research sites to support them with invoicing, revenue collection and CTMS management. We manage the system, load new protocols and budgets, and reconcile payments. We invoice and follow-up. We provide sites with the financial expertise to get paid for all the work they do.


Elligo 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 EHR data and applies a proprietary, prescreening process to match protocol-eligible patients for clinical studies..

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