CROWN offers an ideal opportunity to showcase leading clinical services, technologies and products to an audience of senior-level decision-makers. For more information on the sponsorship and exhibition opportunities, contact Andrew Sinetar at 212-400-6237 or firstname.lastname@example.org
4G Clinical is a leader in randomization and trial supply management (RTSM) for the global life sciences industry, offering the only fully cloud-based, 100% configurable and flexible solution utilizing natural language processing (NLP) and integrated supply forecasting. 4G Clinical is headquartered in the Boston corridor of Wellesley, MA, with offices in Europe and Asia. Learn more about 4G Clinical at www.4gclinical.com.
August Research is an American-owned CRO offering clinical trial services in Central and Eastern Europe. With over 15 years of experience in the region, we offer expertise in a variety of therapeutic indications and study phases. Our team of experienced CRAs, Project Managers and Regulatory specialists provide the highest quality of service while still being flexible to meet our clients’ needs. Realize the benefits of working in Central and Eastern Europe with August Research.
Deep 6 AI® finds more, better-qualified patients for clinical trials in minutes rather than months. Using artificial intelligence on medical records, we accelerate patient recruitment exponentially, getting life-saving cures to people faster.
eClinical Solutions is a leading provider of cloud based enterprise software and software-driven clinical data services. The elluminate® Clinical Data Hub provides life sciences companies with greater control of their clinical trial data within one platform for all data sources, from aggregation through to standardization, visualization and preparation for submission. elluminate software and data driven services have been used by more than 80 life sciences companies on over 400 clinical trials to reduce cycle time and improve data quality. For more information, visit www.eclicnicalsol.com, or contact us at email@example.com.
ERT is a global data and technology company that minimizes uncertainty and risk in clinical trials so that customers can move ahead with confidence. With nearly 50 years of clinical and therapeutic experience, ERT balances knowledge of what works with a vision for what’s next, so we can adapt without compromising standards.
Powered by the company’s EXPERT® technology platform, ERT’s solutions enhance trial oversight, enable site optimization, increase patient engagement and measure the efficacy of new clinical treatments while ensuring patient safety. Since 2014, more than half of all FDA drug approvals came from ERT-supported studies. Pharma companies, biotechs and CROs have relied on ERT solutions in 10,000+ studies spanning more than three million patients to date. By identifying trial risks before they become problems, ERT enables customers to bring clinical treatments to patients quickly — and with confidence.
GlobalCare brings more than 100 years of experience in the clinical trials and home healthcare industries supporting over 400 studies in over 50 countries by effectively delivering high-quality and convenient clinical trial services in the home or alternate-site setting. GlobalCare maintains a global clinical network of ambulant clinicians and country coordinators and operates offices in North America and Europe. GlobalCare supports all phases of clinical trials in a variety of therapeutic areas, genomics and personalized medicine in all age groups. GlobalCare also provides a variety of site support services. Please call today at +1 (847) 282-3280 or e-mail us at firstname.lastname@example.org.
Inato helps biopharmaceutical companies accelerate clinical trial recruitment by making data-informed decisions.
They’ve built a data-driven site selection platform for sponsor’s teams, combining multiple data sources to provide personalized site insights, modelization of recruitment scenarios, and advanced investigator relationship management capabilities.
They have conducted pilots on pivotal trials in a wide range of therapeutic areas (oncology, pulmonology, rare diseases etc.) and have now deployed their solution on all clinical trials (>100 over next 12 months) for top-tier pharma companies.
inSeption’s insistence upon securing the “right” people to integrate into a true partnership alliance with its clients eliminates the vulnerability so often felt by operational leaders faced with evaluating traditional outsourcing options. inSeption’s core competency of identifying and securing the most experienced and proficient professionals builds the crucial foundation of a successful drug development program. Actively collaborating with its clients to custom design, hand select and assemble high-performing project teams empowers inSeption to tailor its services specifically to meet the needs of their programs. The inSeption model provides increased control, full transparency of project deliverables and timelines, and significant operational and cost efficiencies.
IQVIA™ Commercial Compliance is the industry’s trusted name to deliver scalable, end-to-end technology solutions, strategic guidance and best in-class managed services, to effectively meet the demands of global compliance.
Streamline and automate HCP/HCO interactions, efficiently manage global transparency reporting, mitigate risks, reduce costs, increase efficiencies and generate strategic insights from data to improve decision making.
Learn more at iqvia.com/commercialcompliance.
Founded in 2010, KPS is a Functional Service Provider (FSP) offering Clinical Monitoring Oversight, Clinical Monitoring and Project Management solutions to the biopharmaceutical industry. With 335 employees in 28 countries, KPS offers a flexible, scalable solution that identifies and hires experienced, high-quality resources that are fully dedicated to our Sponsors at a cost that represents >35% reduction in professional fees from that of traditional CROs.
myClin is the world’s first Clinical Oversight Platform, offering state-of-the-art collaboration channels and the most documented, data-driven clinical trial oversight available. Along with patients, sites are at the heart of your studies right? Really? Isn’t it time we made site participation in our studies easier? Real-world, measurable compliance with study procedures is closely correlated with high site engagement – so give sites a software experience that they love to use.
myClin acts as a real-time, central team document repository which streamlines study communication and can be tagged according to the TMF reference model 3.0. The common challenges our customers are addressing with myClin are:
NCGS, Incorporated is an international full-service CRO, providing clinical development support to pharmaceutical, biotechnology, medical device, and diagnostic companies. NCGS’ business model is discernibly different from the industry standard: Utilizing highly tenured staff, NCGS consistently delivers studies on time, within budget and of the highest quality. NCGS is a WBENC-certified diversity supplier, has been in operation for more than 30 years, and supported the approval or expanded labeling of 34 products with zero 483s.
NCGS understands that the CRO-Sponsor relationship is one of shared vision, complementary expertise, and trust. NCGS’ team understands the demands of the life science industries, seeking ways to make each clinical effort more quality-based, thorough, timely and cost-effective.
NCGS’ mission is to protect research subjects, capture quality data and maintain the integrity of science with the same passion one would protect their own domain. Each staff member is charged to function under the mantras, “This product could easily be used on your parent, sibling or yourself.” and “It is not only our hope for this product, it is the world’s hope for this product.”
Saama Technologies is the advanced clinical data and analytics company, unleashing wisdom from data to deliver better business outcomes for the life sciences industry. Saama’s unified, AI-driven clinical data analytics platform seamlessly integrates, curates, and animates unlimited sources of structured, unstructured, and real-world data to delivering actionable insights across all therapeutic areas. The award-winning platform gives unprecedented real-time visibility into clinical data, enabling sponsors to file New Drug Applications (NDAs) more efficiently to bring drugs to market faster and at lower costs.
Stiris Research – An entrepreneurial Clinical Trial Management company providing Phase I through IIIB full-service support to Biotechnology and Biopharmaceutical companies. We; help you access SRED funding, keep you safe, and help you maximize your IP ROI. Stiris – designed by clinical entrepreneurs, for clinical entrepreneurs.