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
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.
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 email@example.com.
IQVIA 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.
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.
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.”