Sponsors
Marquee Sponsor
http://www.rpsweb.comRPS, The Next Generation CRO, provides comprehensive global Phase II-IV clinical development solutions to the Pharmaceutical, Biotechnology, Medical Device and Diagnostic industries. By combining an experienced clinical research operations infrastructure with the industry's largest resourcing engines, RPS is uniquely positioned to offer our Customers a broad spectrum of outsourcing solutions. These solutions range from globally Embedded functional and cross-functional programs to enhanced global full-service solutions, and are powered by highly experienced project teams providing innovative, seamless, cost-effective and high quality services. With more than 4,000 employees, RPS operates in 64 countries across the globe.
Platinum Sponsors
http://www.incresearch.comWe are a therapeutically focused contract research organization with a high performance reputation for conducting global clinical development programs of the highest integrity. Pharmaceutical and biotechnology companies look to INC Research for a complete range of customized Phase I - Phase IV programs in therapeutic areas of specialty, and in innovative pediatric and women’s health trials. Our Trusted Process® methodology and therapeutic foresight leads our customers to more confident, better-informed drug and device development decisions.
inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing.http://www.inventivhealthclinical.com.jpg "PAREXEL")
PAREXEL knows scientific drug development from end-to-end of the product development cycle: clinical development, integrated technologies, regulatory affairs, market access, and commercialization services. We complement your capabilities with our global reach, strategic insight, deep scientific knowledge, and tactical expertise—providing you support and guidance to secure strategic advantage. Headquartered near Boston, Massachusetts, PAREXEL operates in 67 locations throughout 52 countries around the world, and has approximately 10,850 employees. For more information about PAREXEL International visithttp://www.parexel.com
PPD is a leading global contract research organization providing discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. Through strong strategic alliances and close partnership with our clients, we apply innovative technologies, therapeutic expertise and quality services to help maximize returns on R&D investments and accelerate delivery of safe, effective therapeutics.
http://www.ppdi.com
http://www.ubc.comUBC unites unsurpassed experience in generating real-world evidence of product safety, value, and effectiveness, with the strength of its parent company, Express Scripts, the nation’s largest healthcare company. UBC leads the market in providing integrated, comprehensive periapproval, safety, and commercialization services. Working hand-in-hand with Express Scripts’ specialty pharmacy and specialty distribution organizations, Accredo and CuraScript, UBC is uniquely positioned to seamlessly integrate best-in-class products, services and healthcare data to influence the lifecycle of a product.
UBC brings together renowned epidemiology, risk management and periapproval experts with leading-edge technologies, enabling customized solutions that support an optimized regulatory pathway while maximizing product position in a competitive market.Gold Sponsors
http://www.chiltern.com/Established in 1982, Chiltern is a leading global clinical CRO with extensive experience in the management of Phase I-IV clinical trials across a broad range of therapeutic areas, functional service provision and contract staffing solutions. Chiltern has conducted trials in more than 40 countries, employs 1,400 people globally and offers services in Early Phase, Global Clinical Development, Late Phase, Biometrics, Medical and Regulatory Affairs and Resourcing Solutions. Chiltern prides itself as a development partner that offers flexibility, responsiveness and quality delivery. Further information is available at www.chiltern.com.
ICON is one of the world’s largest providers of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support clinical development - from compound selection to Phase I-IV clinical studies. We have helped to develop 90% of the world’s top 20 drugs and continue to provide exceptional and innovative services to fulfill our clients' clinical trials’ requirements. These services which include clinical research, clinical pharmacology, imaging, laboratory, late phase & outcomes research and resourcing are offered through the expertise of our six global divisions. For more information, please go tohttp://www.iconplc.com
http://www.labcorpclinicaltrials.comLabCorp Clinical Trials is a division of Laboratory Corporation of America(r) Holdings (NYSE: LH), one of the world's largest clinical laboratories with annual revenues of $5.5 billion in 2011 and more than 220,000 clients. LabCorp Clinical Trials supports pharmaceutical companies with innovative laboratory services for their global clinical trial programs. We provide laboratory testing at our wholly owned central labs in Belgium, China, Singapore and the USA - including Phase I-IV trials, esoteric testing, biomarker development and validation, new method development and companion diagnostics.
Associate Sponsors
AMC Health supports clinical trials with biometric telemonitoring, ePRO, medication monitoring, adherence counseling, video eVisits, activity monitoring and appointment reminders. Remote patient monitoring delivers more and better-quality data to improve signal detection, while eVisits reduce subject burden and cost. AMC Health — helping make trials better, faster and cheaper.http://www.amchealth.com
Anolinx is a data-driven clinical research and clinical trials recruitment company. We focus on the front end of the clinical trials process: trial design, feasibility, and patient recruitment. We enable our clients to streamline the clinical trials process and reduce the cost and time to market for new medicines.http://www.anolinx.com
BBK Worldwide is the industry leader in global clinical trial patient recruitment and retention, providing a complete range of products, services, and technology. Founded in 1983 by Joan F. Bachenheimer and Bonnie A. Brescia, BBK has helped to accelerate time-to-market for new treatments, successfully supporting hundreds of studies in more than 70 countries and all major therapeutic areas. Staffed by some of the industry’s principal thought leaders, BBK continually contributes ideas that advance the clinical development cycle. The introduction of shop.BBKWorldwide.com – the first online shopping experience for clinical research professionals – represents BBK’s latest contribution to advancing the industry through sharing knowledge and best practices.http://www.bbkworldwide.com
Bio-Imaging is dedicated to the comprehensive management of medical images in Clinical Trials. We handle every detail from initial study consultation and preparation to imaging data quantitation, independent blinded review and final regulatory submission. We've managed over one million images worldwide for over 100 pharmaceuticals, biotechnology, and medical device companies.http://www.bioclinica.com
BioStorage Technologies, Inc. is the premier, global provider of comprehensive sample management solutions for the bioscience industry. Offering flexible onsite, offsite and hybrid sample outsourcing models for the management of research assets, BioStorage Technologies manages the complete life-cycle of samples. With an expert team of global sample consultants, industry-leading temperature-controlled storage facilities, and state-of-the-art virtual sample management and bioprocessing solutions, the company supports its customers in maximizing opportunities, minimizing risk and reducing costs. BioStorage Technologies, Inc. is privately held and headquartered in Indianapolis with an additional full-service site near Frankfurt, Germany and a wholly-owned division in Singapore. For more information, visit www.biostorage.com or call +1 (866) 697-2675 or +49-6155-898-1011.http://www.biostorage.com
http://www.catalent.comCatalent Pharma Serivces - Tailored solutions from a global leader. With more than 25 years of clinical trial supply experience, we have the resources and expertise to deliver cost effective and time sensitive solutions around the world. Whether you are seeking standalone support or a comprehensive package, we have the right solution for you.
CFS Clinical (CFS) is a specialty provider focused on the business and financial management activities for clinical trials. The company offers a unique blend of contract, regulatory, and cutting edge investigator grant payment management services which operate in unison to accelerate cycle times, manage compliance and risk, and stimulate investigator relationships. With our focused expertise, innovative processes, and integrated technology we are able to provide high quality, cost effective service solutions that address critical study startup and financial issues affecting the clinical trials process. Visit CFSClinical.com.http://CFSClinical.com
http://www.corelabpartners.com/CoreLab Partners is a global independent core lab providing best-in-class centralized cardiac safety services and medical imaging assessment solutions for pharmaceutical, biotechnology, and medical device sponsors of Phase I-IV studies. Our commitment to service quality and scientific excellence is focused on expediting our clients’ drug development programs.
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Clinical Reference Laboratory provides harmonized global central laboratory services throughout the Americas, Europe, Asia, Australia/NZ & South Africa. We perform a full spectrum of laboratory testing including safety testing, biomarkers for efficacy, pharmacokinetic assays, and molecular testing along with providing logistical support locally and globally, study management and data transfers in customer specific format and frequency.http://www.crlcorp.com
Cognizant Life Sciences partners with 27 of the top 30 global pharmaceutical/biotech organizations. We enable business transformation by delivering consulting, analytics, IT and business process outsourcing support. Our comprehensive clinical data management and biostatistics solutions improve clinical outcomes by increasing the productivity, quality and efficiency of the drug development process.http://www.cognizant.com.bmp "Eurofins Global Central Laboratory")
Eurofins Global Central Laboratory
At Eurofins Global Central Laboratory, laboratory science is our sole focus. With over 20 years of experience and scientific expertise, we utilize our global central laboratories to continually attain the most cost effective and efficient solutions for your clinical trial needs. We are dedicated to providing all laboratory testing needed in clinical trials and have developed one of the broadest testing portfolios available in the pharmaceutical industry today. By combining all laboratory testing in one project, we offer synergetic benefits with regard to turnaround time of results, harmonized procedures, logistics and reporting. Eurofins Global Central Laboratory supports its customers with 6 wholly-owned facilities in the United States, Europe, India, Singapore and China. With three central laboratories operating in the Asia-Pacific region, Eurofins Global Central Laboratory is considered as one of the top central laboratory organizations in the world. If required, we extend our global coverage through standardized local central laboratory partners to reduce costs, accelerate logistic timelines, or to accommodate local needs for a given study.http://centrallabs.eurofins.com
Idis has 25 years experience of partnering with pharmaceutical and biotechnology companies to create regulatory-compliant, ethical access to medicines for healthcare professionals and their patients with unmet medical needs. Since 1987, Idis has developed and managed access to thousands of medicines from every therapeutic category, impacting the lives of hundreds of thousands of patients in countries around the world.http://www.idispharma.com
Idis leverages decades of experience, regulatory insight, and a thorough understanding of local and global requirements to create access to medicines at every stage of a product’s lifecycle from pre-approval to market exit, and in times of unexpected production shortages.
The Company’s International headquarters are located in Weybridge, United Kingdom, and the North American headquarters are located in Princeton, New Jersey.
IMS’s Managed Markets Services organization focuses on support for our life sciences clients’ managed markets operational needs, specifically addressing claims adjudication, trade relations, contracting and government pricing challenges. As market conditions intensify, manufacturers require increasingly sophisticated data, analytics and solutions to realize the full potential of their contracting initiatives. IMS provides that insight through advisory, systems implementation and business process services, and analytical tools and information assets. To learn more, visit www.imshealth.com/managedmarketserviceshttp://www.imshealth.com
Incorporated in 1998, Intelsius is a subsidiary of DGP Life Science Ltd, which is headquartered in York, United Kingdom. Intelsius is a global company specializing in the design, manufacture and supply of temperature-controlled and regulatory-compliant packaging solutions for the life sciences industry. With a strong focus on developing environmentally sustainable products and procedures, the company offers solutions to ensure the integrity of customers’ products and samples for better human and animal health worldwide. Intelsius serves a wide range of organizations, including government agencies, leading pharmaceutical, biopharmaceutical and clinical research industries to major laboratories. Intelsius has manufacturing facilities, distribution hubs and local offices situated throughout the world, including North America, Europe and Asia.http://www.intelsius.com.png "Marken")
http://www.marken.comMarken is the leading global clinical supply chain solutions provider dedicated to the pharmaceutical and life sciences industries, supporting over 49,000 investigators in more than 150 countries. Marken integrates Depot and Logistics services into solutions that extend the reach of clinical trials to even the most remote treatment naïve geographies, leveraging decades of experience in the logistics, transport and distribution of temperature sensitive life saving pharmaceuticals, clinical trial supplies and specimen collection. Our team members, technologies and network of facilities bridge the distance between patients and the essential resources of life science companies.
Medpace is a leading global full-service clinical research organization providing Phase I-IV core development for biopharmaceutical and device programs. Highlighted by medical and regulatory expertise, Medpace has developed therapeutically focused teams to execute at all operational levels, providing complete and seamless drug development services. With clinical trial experience in over 40 countries, Medpace creates strategic partnerships to provide the most efficient and cost-effective path to drug development – from program planning and execution to product approval.http://www.medpace.com
Merge eClinical solutions are delivered as a single clinical trial operating platform that is available anywhere, any time. Merge eClinical OS™ is a truly unified platform designed to help clients manage and run studies faster and more cost effectively. Users benefit from the convenience of one operating platform with clinical trial capabilities that can be mixed and matched to build a solid foundation for each trial environment. Built as a pay-as-you-go service, and supporting any trial in any phase, eClinical OS puts study management back in the hands of its users. Any trial. Any data. One solution. For more information, visithttp://merge.com/eclinical
Modernizing Medicine Inc (MMI) builds next generation cloud based electronic data capture technology. MMI"s native iPad powerful Electronic Medical Record (EMR) systems accommodate the specific needs of specialty practices with a 100% structured data approach, built in medical knowledge (no templates or macros), and an adaptive learning engine that learns how each provider practices. MMI currently offers systems for the following specialties, with more specialties on the way; Dermatology, Ophthalmology, Optometry, Plastic Surgery, Cosmetic Surgery, and Orthopedics.http://www.modmed.com
http://www.praintl.comPRA is transforming clinical trials through our people, innovation and transparency. PRA provides personalized service customized to the unique requirements of each study. We serve all phases of pharmaceutical and biotech drug development by combining therapeutic and operational expertise with local knowledge; ensuring that sponsors achieve their long-term goals.
Serving sponsors for 30+ years, we have amassed a level of expertise that has enabled us to work on a variety of compounds, ranging from niche treatments and therapies to blockbuster drugs. Our forward-thinking approach to transforming the clinical trial landscape continues to make a difference to healthcare patients around the world.
Stiris Research, a certified woman-owned Clinical Trial Management organization providing full-service and functional-service support to the pharmaceutical, biotech and medical device industries.http://www.stirisresearch.com
Tata Consultancy Services (TCS)
http://www.tcs.com/clinicalresearchTata Consultancy Services (TCS) is an IT services, business solutions and outsourcing organization that delivers real results to global businesses, ensuring a level of certainty no other firm can match. TCS is a preferred partner for six of the top ten global pharmaceutical companies. TCS provides business process services such as Clinical Data Management, Biostatistics, Medical Writing, Regulatory Reporting and Pharmacovigilance apart from technology services and tools for Clinical trials.
Theorem Clinical Research is a leading midsized provider of comprehensive clinical research and development services with offices in more than 30 countries and a customer base comprised of some of the world's leading pharmaceutical, biotech and medical device companies. A world leader in the most complex medical device and drug-device combination trials in addition to a notable capability in pharmaceuticals and biologics, Theorem has deep expertise in a broad range of therapeutic areas and in all phases of development. Some of the industry's top scientists and most advanced clinical analytics capabilities help ensure smooth-running, successful trials. For a full-service, right-size global research partner, don't think twice. THINK THEOREM.http://www.theoremclinical.com
Since 2004, Trifecta has designed and developed both live and online training for hundreds of clinical trials worldwide, decreasing time for site readiness, accelerating enrollment and improving communication between sponsors, sites and CROs. Utilized by 12 of the country's top 25 pharmaceutical companies, Trifecta's training system is currently in use in 76 countries on studies ranging in size from two sites to more than 1800. With extensive experience providing lighting, sound, staging, and Audience Response Systems around the world, Trifecta currently produces approximately 300 live and online Investigator Meetings every year.http://www.trifectaclinical.com/
Founded in 2007, Tudor Reilly is a healthcare communications specialist, focused on ethical drug development and supporting patient recruitment to clinical trials. Independently owned, Tudor Reilly works with the senior leadership of the pharmaceutical industry as well as key healthcare providers, including academia, government, the UK National Health Service and patient groups. The Tudor Reilly team combines extensive media experience – including senior roles at the BBC, Reuters and Sky News – with scientific insight, a commitment to innovation and rigorous implementation. For more information please visit:http://www.tudor-reilly.com
SAS is the leader in business analytics software and services, and the largest independent vendor in the business intelligence market. As the de facto industry standard for clinical data analysis and reporting, SAS helps organizations improve the effectiveness and efficiency of the entire clinical trials process. SAS is used by 100 percent of the Fortune Global 500® life sciences companies. Since 1976 SAS has given customers around the world THE POWER TO KNOW®.http://www.sas.com- Modernizing Medicine Inc (MMI) builds next generation cloud based electronic data capture technology. MMI"s native iPad powerful Electronic Medical Record (EMR) systems accommodate the specific needs of specialty practices with a 100% structured data approach, built in medical knowledge (no templates or macros), and an adaptive learning engine that learns how each provider practices. MMI currently offers systems for the following specialties, with more specialties on the way; Dermatology, Ophthalmology, Optometry, Plastic Surgery, Cosmetic Surgery, and Orthopedics.http://www.modmed.com
- Founded in 2007, Tudor Reilly is a healthcare communications specialist, focused on ethical drug development and supporting patient recruitment to clinical trials. Independently owned, Tudor Reilly works with the senior leadership of the pharmaceutical industry as well as key healthcare providers, including academia, government, the UK National Health Service and patient groups. The Tudor Reilly team combines extensive media experience – including senior roles at the BBC, Reuters and Sky News – with scientific insight, a commitment to innovation and rigorous implementation. For more information please visit:http://www.tudor-reilly.com
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