47th Annual DIA Meeting Exhibitor Profiles A through I

Beardsworth is an oncology-focused CRO celebrating 25 years of clinical research excellence. Beardsworth partners with each client to provide the best solution-based business model for each project. Global solutions through OncologyOne®. Patient-centric approach, straight talk, strong management & solid metrics result in accurate, trusted study results - on time/within budget. Feasibility and rapid study start-up through Investigator Express. Team of experienced research clinicians (70% medical and/or industry certified) invested in the outcome of each project. Risk mitigation, issue escalation and PMI methodology incorporated into each project plan. Diversity advantage as a Federal CCR registrant and designated Small Business.

Biomedical Systems is a global provider of centralized diagnostic services for clinical trials for Cardiac Safety and Efficacy, Pulmonary Function, Imaging, Neurophysiology and Digital Pathology testing. In addition, the company offers a full suite of pharmaceutical consulting services including Protocol Development per the specific modality, Medical Writing and Statistical Analysis. With offices in North America, Europe and Asia, Biomedical Systems works with over 14,000 clinical sites in 95 countries around the world.

C3i is the leading provider of end-to-end technology services for sponsors and CROs running global clinical trials. C3i's portfolio of business process outsourcing services for EDC, IVRS/IRT, CTMS, and ePRO applications includes: 24x7 multi-lingual contact center, systems integration, technology training, asset management, provisioning, technical site assessments, and application hosting exclusively tailored for the needs of clinical professionals.

Camargo Pharmaceutical Services is an end-to-end drug development services company. Specialized in the 505(b)(2) pathway, Camargo develops successful programs for safety and efficacy in small and large molecules. With more than 150 FDA approvals, Camargo works with companies in 26 countries worldwide to develop comprehensive programs, executing every facet of the plan from formulation and testing the drug product, conducting clinical studies and FDA application submissions. Connect with Camargo on LinkedIn, Camargo’s Blog, or visit www.camargopharma.com.

For more information about Advisor newsletter, books, posters and Q&A cards visit www.canarybooks.com.

Clinical Resource Network (www.clinicalresource.net), a leading provider of specialized in-home and alternate-site clinical services to patients in all phases and therapeutic areas of clinical trials. CRN's services significantly accelerate the pace of clinical trials by leveraging its extensive network of clinical service agencies to increase convenience for patients. CRN helps clinical trial sponsors dramatically improve patient recruitment, compliance and retention as well as increase patient and investigator satisfaction. For more information about our global clinical trial services contact Brent Barnett at 224.533.8548, [email protected].

CompleWare Corporation

CompleWare Corporation, a leader in the use of eTechnology to conduct clinical trials, provides lean eClinical innovation, integration, and quality leading to increased speed and accuracy of data capture, enhanced subject compliance, and controlled study costs. CompleWare is both a full service CRO as well as a technology vendor of ePRO options.

C&R Research, the first CRO established in Korea was incorporated in 1997 contributing to development of CRO industry in Korea and have been grown continuously at high growth rate of CAGR over 30% from 2004 to 2010. From accumulated proven capability, we are No.1 in regulatory clinical trial segment in Korea and we have conducted over 50% of global studies among clinical studies successfully. C&R Research has been growing and expanding continuously as a leading CRO company in Korea based on successful and outstanding performances in a variety of areas in the pharmaceutical, biotech and medical device industries while providing a full range of services in regulatory affair, clinical trial, PMS, data management and statistical analysis services as well as GCP auditing service by meeting international standard strictly.

CTI Clinical Trial & Consulting Services

CTI Clinical Trial and Consulting Services (CTI) is a full service global CRO/consulting company offering a range of services which encompass the entire lifecycle of drug development. Services include regulatory pathway design, clinical trial management, monitoring, data analysis, pharmacovigilance, medical writing, CME, training program development, market analysis and other consulting services. CTI focuses on the specific disease areas of solid organ transplant, hepatitis, infectious disease, end-stage organ disease and regenerative medicine. With its combined expertise of clinical knowledge and market experience, CTI is uniquely positioned to provide extraordinary results.

Headquartered in Dallas, DAC Patient Recruitment Services (formerly D. Anderson & Company) is an affiliate of Imperial—a clinical research support organization with offices in Michigan, Pennsylvania and the United Kingdom. With 19 years’ experience in more than 100 countries and 40 indications, DAC is a single-source provider of comprehensive services targeted to clinical trial sponsors and CROs. Core competencies include strategic site selection, customized patient recruitment and retention, award-winning creative services and global clinical staff training. Additionally, DAC offers certified translations for 115 languages; printing, shipping and global fulfillment. Call (800) 466-1774 or visit www.DACprs.com.

DOKUMEDS is a European CRO providing a comprehensive range of services to more than 80 clients in pharma, biotechnology and medical device industry worldwide. Focus on customer needs, trustful relationships and quality is the core stone of Dokumeds business philosophy allowing to reach the ratio of repeated business up to 80%.

Topical formulation development has been Dow Pharmaceutical Sciences' successful focus for 33 years. Dow helps clients with early feasibility studies through proof of concept in man and on to NDA. Over one third of all topical prescription dermatological products approved by FDA 2005-2010 were developed by Dow.

Dow provides a full range of product development services for pharmaceutical and biotechnology clients in the dermatologic, ophthalmic, women's health, topical pain, and topical anti-infectives arenas. Services include formulation development, in vitro tissue penetration studies, analytical services, regulatory strategy and submissions, and GMP clinical manufacturing and labeling.

www.clinplus.com

DZS Software Solutions, Inc. (www.clinplus.com) is a privately held company founded in 1996 providing clinical trials management software for data management, electronic data capture, medical coding and data analysis and reporting to the biotech and pharmaceutical and medical device industry worldwide. DZS Clinical Services (www.dzs.com) division provides a variety of clinical outsourcing services using ClinPlus software.

Our professional staff is qualified to conduct the most complex of clinical trials. We have a local Independent Investigational Review Board that provides rapid decisions on study reviews and approvals, we also could use central IRB per sponsor require.

Getz Pharma Research is a Contract R&D Organization with facilities located near Nuvi Mumbai, India. We specialize in providing world-class product development services, for all types of dosage forms, to pharmaceutical companies worldwide. Whether developing targeted enhancements for existing products, advancing new formulations or developing of innovative new products from the ground up, we are fully committed to deliver to our clients, rapid, cost-effective, and high quality services in a cGMP environment. With a presence in the US as well, we are able to offer turn-key services from API development through final product manufacture. Please visit us at Booth #2015 to learn more about our capabilities and added-value services.

Greenphire is the industry leading provider of clinical payment and communication technology solutions. Greenphire’s ClinCard and ClinicalGPS solutions were designed specifically for the clinical research environment, and are configurable to the specific requirements of each individual clinical study. Greenphire strives to provide the most dedicated service to our clients, including sponsors, study teams, site coordinators, investigators, and CROs.

Inmark has been offering innovative packaging solutions for over 30 years and we are a Global Supplier of temperature control, dangerous goods and clinical trial packaging. World class design testing and validation facilities along with 20 years of in-depth industry experience in cold chain technology through our alliance with Softbox Systems have created innovative award winning designs for thermal packaging now used globally. Our dangerous goods regulatory development includes a delegate at UN Sub-Committee of Experts on the Transport of Dangerous Goods in Geneva. The clinical trials packaging systems we developed and implemented for the central laboratories in North America, Europe and Asia are now the industry standard.

To learn more, please call us at 0039 (0362) 573128 or visit our website www.innopharma.it.