2020 Exhibitor Information
Advarra is the premier provider of IRB, IBC and global research compliance services in North America. By combining the mutual strengths of Chesapeake IRB and Schulman IRB, Advarra delivers exceptional client service, innovative technology and unmatched regulatory expertise, providing integrated research compliance capabilities to help make research altogether better.
Bayer is a global enterprise with core competencies in the Life Science fields of health care and agriculture. Its products and services are designed to benefit people and improve their quality of life. At the same time, the Group aims to create value through innovation, growth and high earning power. Bayer is committed to the principles of sustainable development and to its social and ethical responsibilities as a corporate citizen. In 2016, the Group employed around 115,200 people. For more information, go to www.bayer.com.
Bio-Optronics is the creator of Clinical Conductor, the leading CTMS for collaboratively managing multiple clinical trials and sites. Used by more research sites around the world than any other CTMS, Clinical Conductor is managing over 40,000 studies. Clinical Conductor is part of the CCTrialSuite, a comprehensive set of integrated, patient-centric clinical research management and eClinical products available from a single supplier that streamline research operations, ensure compliance and enhance research business growth. Adding to the power of Clinical Conductor in the suite are a growing set of new solutions, including Part 11 compliant CCeReg document management, CCeSource real-time data capture, mobile friendly CCeConsent, instant payment CCPay and 2-way texting CCText solutions that will have the most seamless CTMS integration in the industry. https://bio-optronics.com/
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.
Clincierge® improves clinical trial performance by reducing barriers to participation, enhancing enrollment, and minimizing drop-outs. Our expertise and services lessen burdens on patients, caregivers, and sites while improving communications and coordination. We help keep studies on schedule, on budget, and data quality high, while making patient concerns a priority. clincierge.com
As regulatory requirements expand and clinical trials grow more complex, it has become increasingly burdensome for research sites to manage documentation. Complion’s document and workflow management platform improves efficiency, compliance and transparency for research sites and sponsors.
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.
Cognizant partners with biopharmaceutical and med-tech companies to develop strategies and apply solutions to healthcare challenges across the value chain. Our services and products, including the Shared Investigator Platform (SIP), 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/life-sciences-technology-solutions
As regulatory requirements expand and clinical trials grow more complex, it has become increasingly burdensome for research sites to manage documentation. Complion’s document and workflow management platform improves efficiency, compliance and transparency for research sites and sponsors.
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.
GlobalCare Clinical Trials, LLC is the leading global provider of ambulant healthcare services for clinical trials. GlobalCare provides innovative, GCP-compliant services for biopharmaceutical companies by conducting selected study visits at locations convenient and comfortable for the patient when travel to the investigator site is not practical. GlobalCare’s traveling clinicians provide patients with a convenient way to participate in trials regardless of study duration, frequency of visits, their disease state or distance to the study site. Additionally, GlobalCare’s patient-centric approach helps to accelerate patient recruitment and improve study patient compliance and retention. www.globalcarect.com
Greenphire is the global leader in financial software for clinical trials. Greenphire’s best-in-class solutions optimize clinical trial performance by streamlining financial and logistical workflows from sponsors and CROs to sites and patients. Greenphire’s ClinCard and eClinicalGPS solutions easily handle any type of trial design and complexity, resulting in more accurate and compliant payments globally for both sites and patients. ConneX is the most personalized clinical trial travel solution designed specifically to meet the recruitment and retention goals of domestic and international clinical trials. The choice of industry leaders worldwide, Greenphire provides better performance and better data, resulting in better trials. www.greenphire.com.
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
ICON is a global provider of outsourced drug development services to biopharma, medical device, government, biosimilar and generic organisations. We offer a full range of clinical, consulting and commercial services that range from trial design to full study execution, and from clinical to post-market commercialisation. Our services are supported by in-depth therapeutic and regulatory expertise and market-leading technology and analytics. We are the only full service CRO that offers the knowledge, software and systems for adaptive trials.
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.
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 is the leading global provider of cloud-based solutions for clinical research in life sciences, transforming clinical development through its advanced applications and intelligent data analytics. The Medidata Clinical Cloud™ brings new levels of productivity and quality to the clinical testing of promising medical treatments, from study design and planning through execution, management and reporting. www.mdsol.com
Medix Clinical Research offers workforce solutions and consulting services for sites, sponsors and CROs. Our in-house clinical research expertise will help you enhance operational strategy, maximize financial efficiency and bolster your talent pipeline.
Oracle Health Sciences is the market leader in clinical solutions delivering transformative value for R&D in a modular, integrated, secure and high-performing cloud environment. We enable trial sponsors and CROs to optimize trial efficiency while reducing cost and risk from startup through submission; collect, deliver, and analyze higher-quality data faster; and help ensure patient safety during clinical trials and post-marketing surveillance. www.oracle.com/healthsciences.
At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety, and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world’s best-known consumer health care products. We collaborate with health care providers, governments, and local communities to support and expand access to reliable, affordable health care around the world. For more than 150 years, Pfizer has worked to make a difference for all who rely on us. www.pfizer.com
PRA Health Sciences delivers innovative drug development solutions that improve patients’ lives. Our people are passionate about clinical research, working tirelessly to provide quality results. We offer exceptional experience across all phases and therapeutic areas and a broad spectrum of solutions, ranging from full-service clinical development to a pioneering embedded model. With 16,000+ employees covering 90+ countries, we bolster an impressive global presence with keen local insights. Our project teams harness their understanding of local regulations, standards of care and cultural customs to effectively align our approaches with each study’s unique goals. At PRA, we love what do because we are making a difference in the lives of patients and their family members worldwide. Over the years, we have contributed to the development of numerous drugs now available to countless patients. From our scientific and medical experts to therapeutically aligned project managers and monitors, we provide the commitment and expertise needed for today’s complex study. www.prahs.com
RealTime Software Solution is a global leader in SAAS-based Clinical Trials Management Systems for Sites, Sponsors, and CROs. RealTime is also the only CTMS vendor that can offer a complete suite of solutions into a seamless platform, SOMS (Site Operations Management System). SOMS includes the industry-leading CTMS, SitePAY, TEXT, eDOCS, and eSOURCE which is accessible through an easy-to-use MobileAPP. RealTime also has the most advanced multi-site and site network enterprise systems available anywhere.
Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible. For more information, please visit www.roche.com.
Sanofi, a global healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients’ needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new Genzyme. Sanofi is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY). www.sanofi.us
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.
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.
Trifecta is a global leader & trusted partner with deep experience in clinical trial technology solutions for leading pharmaceutical, biotech and clinical research organizations. Trifecta offers clinical trial solutions including: Online/On-Demand Investigator Training, Live & Web-Based Investigator Meetings, Safety Letter Delivery and Document Exchange. To learn more, please visit www.trifectaclinical.com.
Veeva 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. www.veeva.com
VirTrial has a stable, long-standing virtual care platform customized for clinical trial use with both patient and site needs in mind. VirTrial is transforming the use of telemedicine in the clinical research industry by offering a patient management program that combines video, text, and email for clinical trial sites to easily and conveniently address specific patient and/or study needs in a secure environment. The platform can be used on any device and at any site. The company vision is to replace 25-40 percent of standard clinical trial visits with virtual visits to create hybrid studies. This model is best suited for Phase III and IV studies, rare diseases and to replace traditional telephone calls within a protocol. VirTrial enables higher performance by clinical trial sites, greater accessibility to trials for patients, and improved outcomes for pharmaceutical companies. Working together we can bring better medications to market more quickly. https://www.VirTrial.com.
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.
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 is the leading provider of knowledge-based solutions that measurably improve the ROI of clinical research. For over fifty years, WCG has protected the rights and well-being of clinical research participants, fueling progress by keeping volunteers safe. By protecting people, the company has gained unique insight into every aspect of clinical trial operations and collected independent, verifiable data from over ninety percent of the world’s trials. Today, WCG is using those insights to help our clients make better, more informed decisions about the conduct of their trials. Applied to a single research study–or even more effectively, across an entire research program–WCG’s data-driven solutions have been proven to accelerate timelines, reduce costs, and increase the safety of clinical research. By removing many of the operational barriers to success, WCG is helping to maximize the value of clinical research.
AbbVie is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the world’s most complex and critical conditions. The company’s mission is to use its expertise, dedicated people and unique approach to improve treatments and advance health solutions for people around the world. www.abbvie.com
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.
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.
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 APAC that work across the Healthcare sector. With separate divisions and dedicated consultants for the markets we serve ensures a professional and intelligent approach in both permanent and interim solutions.
Boehringer Ingelheim is committed to improving lives and providing valuable services and support to patients and their families. Our employees create and engage in programs that strengthen our communities. Since its founding in 1885, the company has remained family-owned and today creates value through innovation for three business areas including human pharmaceuticals, animal health and biopharmaceutical contract manufacturing. www.boehringer-ingelheim.com
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.
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! www.breezectms.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.
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 https://clinasyst.net to request a demo and find out why more and more sites are choosing ClinasystNG!
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. www.clinicalresearchbilling.com
Elias Associates is an executive search firm that specializes in the Pharmaceutical, Chemical, Medical Device, Biotech, Consumer Products, Food, Automotive, Manufacturing and Plastics Industries. We have over 20 years experience in the placement of EHS, Supply Chain, Quality, Engineering, Finance, and Human Resources professionals. As members of 3 major nation-wide networks (Top Echelon, Inter-City Personnel Associates, NPA, The Worldwide Recruiting Network) we have access to thousands of candidates to help fill your recruiting needs.
Exostar is the cloud platform of choice for secure enterprise and supply chain collaboration solutions and identity and access management expertise. We are forging strong connections between people and technology and partner organizations.
Florence advances clinical trials with through software for managing document and data flow between research sites and sponsors. Florence eBinders is trusted by 2,000+ research teams for eRegulatory/eSource management, and Florence eHub is revolutionizing site-sponsor connectivity in a shared workspace for startup, monitoring, and quality control.
GlaxoSmithKline – one of the world’s leading research-based pharmaceutical and healthcare companies – is committed to improving the quality of human life by enabling people to do more, feel better, and live longer. www.gsk.com
Headlands Research is a globally integrated clinical trial site organization with a mission to dramatically improve the clinical trial process. Our group of exceptional sites focuses on large volume recruitment of diverse and specialty patient populations while delivering the highest quality data.
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 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 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 Susanna Keilman (727) 544-4842, email@example.com.
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.
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 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 provides comprehensive drug development capabilities to help clients get their new and innovative drug treatments into the hands that need them most. We simplify the journey to market through our global regulatory expertise, Phase I-IV clinical research services, integrated eClinical technologies, and commercialization services. For more information, visit www.PAREXEL.com.
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.
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 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 Lance Nickens at firstname.lastname@example.org 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.
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.
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.