2018 Exhibitor Information

 

2018 Premier Exhibitors

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 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

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.

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.

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.

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.

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™
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-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

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.

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, eSource, CTMS, eTMF, and study start-up to unify clinical data management and clinical operations. Veeva has more than 500 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

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

Schulman IRB and Chesapeake IRB have merged to create Advarra, the premier provider of IRB, IBC and global research compliance services. By integrating our innovative technology and proven regulatory expertise, Advarra helps ensure the highest standards of human research protections. Advarra supports all research phases across all major therapeutic areas.

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.

From paperless eSource data capture to electronic budget management, site recruitment and regulatory document management solutions, ACS360 is built for site efficiency. See why more sites prefer paperless studies with ACS360.

 

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 tap into this active network of engaged patients. 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

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

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.

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

 
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 provides sponsors and CROs with experienced and successful clinical research sites located throughout the US. The network consists of 22 research groups, 65 site locations and 200 investigators. The size of our network grants us a unique perspective to understand the capabilities of each PI and site which allows us to match sponsor/CRO studies with sites that have the correct combination of PI, staff, facility 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 Chris Heironimus (727) 544-4842, chris@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.

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.

With headquarters in the US and UK, Myoderm is a global leader in the sourcing, distribution, and management of pharmaceutical products and supplies for clinical trials, including biosimilar research. With an extensive network of qualified manufacturers and suppliers, they specialize in accessing medications in all therapeutic classes and dosage forms – even the most difficult to obtain. Through their deep expertise, innovative approach, and commitment to personalized service, Myoderm provides the optimal supply solution for clients around the world. Visit www.myoderm.com

 
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

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.

The platform developed by Research Hive shortens the development timeline for investigational treatments. Research Hive helps physicians efficiently and effectively identify patients and communicate with their team about potential research subjects, among other things. Improving Physician confidence in their enrolling protocols is one of the most effective ways to improve their team’s enrollment rate.

 

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.

Splash Clinical, a wholly owned subsidiary of Teuteberg, Inc., is a global marketing services company specializing in Online and Social Media Marketing for Clinical Trial Patient Recruitment. We combine our extensive knowledge of online and social media marketing with rich analytics to create highly targeted campaigns that reduce the time and expense required to recruit patients. You can trust that our quality, knowledge, and customer service will help your clinical trial succeed.

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

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.

ThreeWire

ThreeWire is a global patient recruitment, enrollment, retention and management provider for the pharmaceutical, biotech and medical device industries. Our proven, customized, centralized and site-based service offerings provide valuable solutions and measurable outcomes for sponsors, CROs, sites and patients in North America, Europe, the Middle East and Latin America.

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.

Investigator payments and site contracting have long been a thorn in the side of sites, sponsors and CROs. Led by industry pioneers in this space and motivated by promoting site sustainability and trial efficiency, the experts of Transcend Trials invite you to join them in driving change by leveraging their technology-enabled services powered by Medidata Payments.

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

  

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, eSource, CTMS, eTMF, and study start-up to unify clinical data management and clinical operations. Veeva has more than 500 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

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

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