We would like to thank the exhibitors that will be joining us during the 5^th Annual Site Solutions Summit.  

During the Summit they will deliver presentations to our attendees during the Exhibitors Breakfast, join us in discussions during our sessions and host a cocktail reception.  

At the Site Solutions Summit they are not "just an exhibitor".  They are an integral part of the team of which attendees will benefit from their knowledge, products, services and Summit participation.

Platinum Exhibitors
 

Bio-Optronics develops, deploys, and operates software products and custom information technology solutions to help healthcare professionals manage and optimize workflow, thus enhancing quality, productivity, and patient and staff satisfaction.  For 25 years, Bio-Optronics has demonstrated leadership in innovation, expertise in workflow and integration, and a singular approach to unparalleled customer service. The Clinical Conductor^TM product family, used in over 600 sites around the world, provides comprehensive workflow solutions for clinical trials, including clinical trial management systems for investigative sites, academic medical centers and contract research organizations.  For more information please visit our website at http://www.bio-optronics.com/.

Since its founding in 1992, Campania has been dedicated to providing specialty insurance products and services to the healthcare community. Our clinical trails insurance program is specifically designed for clinical trials physicians and sites. To find out more about our customized insurance policies, please contact us at 800-831-9506 or find us online at http://www.thecampaniagroup.com/.

Established in 1993, Chesapeake Research Review, Inc. is a leading provider of IRB Services and consultative support in the area of human subject protection.  Fully AAHRPP accredited, CRRI is committed to meeting the quality and timeline requirements of our clients' fast-paced development schedules.  Our expertise spans the entire spectrum of human research. To find out more, please contact Jeff Wendel 410-884-2900 or visit our website at http://www.chesapeakeirb.com/.

ClinicalRSVP is a cost-effective commercial web-based tool for Sites. It provides a registry to validate subject wash-out periods, allowing participating sites to improve enrollment accuracy in sponsored clinical trials. ClinicalRSVP is administered by Independent Data Integrator (IDI), a company specializing in IT and Database Solutions within the clinical trials industry. Established in 2008, IDI was created with the goal of improving clinical research integrity and participant safety through information technology services. To find out more, contact Darran Boyer at Darran.Boyer@clinicalrsvp.com or visit our website at http://www.clinicalrsvp.com/

ClinForce is a provider of resource solutions offering traditional contract staffing, direct recruiting, and functional outsourcing services to the clinical research industry. For nearly 30 years, ClinForce has introduced talented clinical research professionals to the organizations in need of their skills, and is one of the few national staffing firms addressing the need for experienced Clinical Research Coordinators. Our creative resource solutions include custom-recruited project teams dedicated to functional tasks for specific clinical trials or portfolios of clinical studies. To discuss your specific objectives, contact Colleen Dureau-Inzerillo at 800-964-2877 or cdureau@clinforce.com.

 

Clinical Financial Services is the industry's only company focused exclusively on the financial management of clinical trials. Through unique business process outsourcing capabilities, the company empowers sponsors, clinical research organizations, and investigative sites to transform the way they handle the complex financial activities required to initiate and successfully complete clinical trials.  Our skilled professionals & proprietary systems for Investigator Grant Payments and Contracts enable sponsors to improve site relationships, focus on core competencies, reduce cycle times & cost, and obtain unparalleled reporting capabilities for themselves and their sites.  For more information about CFS, please contact Kevin Williams at kwilliams@clinicalfinancialservices.com or visit our website at http://www.clinicalfinancialservices.com/

 

IntegReview Ethical Review Board is an independent IRB.  Established in 1999, IntegReview applies ethics and integrity to research while accelerating the IRB process with technology, offers multiple weekly meetings, two-day turnaround, expert reviewers, flexible personal service, and knowledgeable/available staff.  IntegReview achieved full AAHRPP accreditation in June 2007.  To find out more about our services, contact Melissa Meyer, Director of Business Development at (512) 326-3001 or mmeyer@integreview.com and please visit our website at http://www.integreview.com/.

Payoneer is a simple and powerful online payment distribution solution that is moving patient reimbursements into the digital era.  Established in 2005, Payoneer provides the most secure, fast and cost-effective worldwide patient reimbursement solution.  Payoneer enables CROs, Investigators and Sponsors to deliver compensation payments to clinical trial subjects at home and abroad, utilizing co-branded prepaid MasterCard® cards.  To find out more, contact Mike Nevin at 484-368-3009 or visit our website at http://www.payoneer.com/. 

StudyManager is an industry-leading provider of Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) solutions to organizations who manage or conduct clinical trial research. Since 1993, we have been making the process of managing clinical trials faster, easier, and more efficient for research sites, hospitals, study sponsors, and CROs. To find out more, please contact Sue Blecman at sueb@stuydymanager.com or visit our website at http://www.studymanager.com/.

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 1,800 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 RADIUS365^TM, 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 the sets TPRA apart from other competitors is that all of these services are performed by TPRA's own IN-HOUSE staff with no outsourcing which offers its clients greater flexibility, accountability and cost-efficiencies than other competitors.  For more information about TPRA services and capabilities please visit our company website http://www.patientrecruiting.com/.

TrainingCampus.com is an international electronic education network that provides a global network of products, services and specialty providers to healthcare and clinical research, sponsors, CRO, sites.  Established in 1999, TrainingCampus.com has standardized the delivery of the NIH Stroke Scale training and certification program, created the first international electronic education network and created the first business-to-business electronic network for clinical research organizations.  To find out more, contact Al O. Pacino II at 512-302-3113 or visit our website at (http://www.trainingcampus.com/). 

Goodwyn IRB has evolved beyond traditional model of IRB review and oversight, generating value beyond the prevailing limits.  Established in 1999, all of our activities are organized around enhancing the welfare of everyone we contact.  From attention to the smallest detail of making your day easier, providing comprehensive reporting, faster activation and enhanced performance of investigative sites to the protection of human research participants, our choice to manifest excellence affects the lives of all.  To find out how, contact Mr. Martin Frazier, our Director of Client Relations, at 919-803-5322 or  visit our website at www.GoodwynIRB.com <http://www.GoodwynIRB.com>.

Aspire IRB, a fully AAHRPP accredited Independent Review Board, is committed to the highest level of human research protection with an emphasis on flexibility, efficiency and a commitment to customer service. Aspire provides customized IRB services to meet the unique needs of our clients in all phases of clinical research with expertise in large multicenter studies and Phase I studies. Aspire’s A.S.A.P. web portal provides 24/7 access for document retrieval and approval status review.

Aspire IRB, founded in 2004, is based in San Diego, CA and serves Pharmaceutical & Biotech companies, CROs and Study Sites in all 50 states and Canada. For additional information,  please contact John Bancroft, Director of Business Development at (619) 469-0108 (john@aspire-irb.com) or visit our website at www.aspire-irb.com.

Site Management Solutions (SMS) is a sister company of Clinical Site Services that helps identify the right trials for sites. SMS has established relationships with pharmaceutical companies and CROs and is aware of currently recruiting studies in the planning stages. While there are other companies offering similar services, investigative sites prefer SMS because of the following:

1. Non exclusive agreements
2. Flat fee based pricing and not per patient financial commitments
3. Discounts for working with our partner companies
4. Training and site setup for physicians looking to enter clinical research

Please fill out our online form (SMSclinical.com/form.html)and we will contact you when we have located studies that meet both your research interests and facility capabilities.

What is goBalto?
goBalto is a small team that creates simple, focused software for the global drug trial industry. Our products offer drug trial sponsors the simplest possible way to start clinical studies on the web.

How we help:
We believe the existing process of starting clinical studies, are – Too complex. Too manual. Too inefficient. Whereas existing solutions focus on managing ONGOING studies, our product goes to where the problem begins – the clinical study STARTUP process. Our products want to automate and bring efficiency to the study startup process.

Founded in 1994, CenterWatch is a trusted source and global destination of clinical trials information for both professionals and patients. CenterWatch provides a wide variety of information services including grant leads for investigative sites; business development leads for contract service providers; postings of career opportunities; listings of clinical trials actively seeking patients; advertising and promotional opportunities; and proprietary business analysis and data about the global clinical trials industry. Visit www.centerwatch.com.

The Biomedical Research Alliance of New York (BRANY) is an Institutional Review Board (IRB) and Investigator Site Alliance that provides  independent and central IRB, Institutional Biosafety Committees (IBC), educational, consulting, site identification and administrative services to sponsors, CRO's, and investigative sites. 
Established in 1998 by five academic medical centers, BRANY was the first IRB in the state of New York to be AAHRPP accredited and is able to offer its partners a turnkey solution for expedited site identification and study start-up, including a single contract, IRB and budget. To find out more, contact Carmela Houston-Henry at (516) 470-6979 or visit our website at www.brany.com.

 Gold Exhibitors

D. Anderson & Company is a global leader in patient recruitment and retention for clinical trials, with experience spanning 18 years, 66 countries and over 40 therapeutic indications. DAC’s site-focused services, clinical range and creative ingenuity set it apart from competitors. For more information, visit dandersoncompany.com or call 800.466.1774.