RPS, 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.
Covance, with headquarters in Princeton, New Jersey, is one of the world’s largest and most comprehensive drug development services companies, with annual revenues greater than $2.2 billion and more than 11,000 employees in over 60 countries.
With the most comprehensive portfolio of preclinical, clinical development and commercialization services, Covance provides industry-leading services, the world’s largest central laboratory network, and a global team of clinical trial and commercialization experts.
CTMS, Inc., a privately held CRO, provides the complete scope of clinical trial management, data management, regulatory and feasibility services for the pharmaceutical, bio-tech and medical device industries. Our full-service and task-based capabilities extend to clients throughout North America and Europe. Our metrics reveal our distinctives, a few of which are summarized below:
96% of all studies have been completed without a CTMS-initiated Change in Scope
Our satisfied client repeat and/or referred business averages 97%
Company-wide cumulative retention rate averages 94% for the last 5 years.
Extraordinarily low database error rate of .0007536
Since 1989, CTMS has provided quality-centered services to Top 10 pharmaceutical, biotechnology, mid-sized and specialty pharma companies. Discover why CTMS is A Refreshingly Different CRO.
We 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.
PharmaNet Development Group
PharmaNet Development Group, a recognized leader of global drug development services to the pharmaceutical, biotechnology, generic drug, and medical device industries, provides comprehensive capabilities in Phase I-IV clinical development, bioanalytical and bioequivalence services, regulatory, staffing, and therapeutic solutions. For the applied knowledge and intelligent solutions needed to accelerate drug development programs of all sizes around the world, PharmaNet works for you.
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.
Quintiles is the only fully integrated biopharmaceutical services provider offering clinical, commercial consulting and capital solutions worldwide. We help customers manage change, navigate risk and seize opportunities in the new health landscape. Quintiles' more than 24,000 talented, engaged employees in nearly 60 countries deliver on promises to customers every day, working with an unwavering commitment to patients, safety and ethics.
As a pioneer in biopharmaceutical services, Quintiles has helped develop or commercialize all of the top 50 best-selling drugs. Quintiles is consistently cited as one of the most favored contract research organization (CRO) in independent surveys of the biopharma industry.
i3 is a global business providing integrated scientific strategies and solutions throughout the biopharmaceutical product lifecycle. Our unique combination of products, services and knowledge helps companies gain sharper insights that lead to better patient care.http://www.i3global.com
Paragon Biomedical, Inc.
Paragon Biomedical is a woman-owned CRO providing Phase I-IV clinical services to pharmaceutical, biotechnology, and medical device companies. With offices and staff in the United States, United Kingdom, and India, we provide full-service support across key therapeutic areas, including cardiovascular, endocrinology, metabolic, infectious disease, respiratory, and oncology. http://www.parabio.com
To compete in today’s market, a CRO has to invest in infrastructure and technologies. But Paragon’s leaders also know that success is linked to the people who form the project team. Our focus on people has resulted in 14% annual average turnover and project team stability that conserves Sponsor resources.
Bilcare Global Clinical Supplieshttp://www.sharpclinical.com
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.
Cmed is a full service CRO combining world-class 21st Century technology with exceptional industry experience that offers a unique approach to clinical research and data capture/management that delivers real advantages to its clients. Cmed has engineered and patented a single database system to handle all aspects of the acquisition, management, review and reporting of clinical data program level. From its offices in the US and Europe, Cmed has provided its clients with high quality services and products at competitive prices.
COAST IRB, LLC
Coast Independent Review Board (IRB) provides ethical and thorough review services for clinical drug trials. We assist clients in overcoming common obstacles such as turnaround time and quality with personalized services and efficient communication. At Coast IRB, we take pride in exceptional service and our perfectionism pledge, setting us apart from other IRBs.http://www.coastirb.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
Essential provides experience-driven patient recruitment and contract research organization (CRO) services that help pharmaceutical and biotech companies achieve quality clinical trial outcomes with greater control over timeline and budget. Our two offerings provide independent and integrated services with a demonstrated commitment to personalized service and unparalleled professional qualifications.
Eurofins Global Central Laboratory
With over 20 years experience, Eurofins Global Central Laboratory serves the pharmaceutical industry, providing unsurpassed quality in laboratory testing, while integrating specialized laboratory services into one project. Eurofins Global Central Laboratory owns laboratories in Washington DC, Breda, Singapore, Shanghai, and Bangalore (May 2011). Discover. Experience.
Gentiae Clinical Research
Formed in 2001 as the for-profit extension of the Ischemia Research and Education Foundation (IREF) – an organization with 20 years of experience in cardiovascular clinical studies – Gentiae is a global leader in comprehensive cardiac safety assessment. Gentiae delivers centralized ECG core lab and imaging services to clients whose clinical trials demand the highest levels of experience and quality clinical interpretation in the analysis of their drug's cardiac safety and functional risk. Leveraging its industry-leading reproducibility and clinical experience, Gentiae is able to deliver tangible value to clients through efficient, cost effective cardiac safety and functional studies in all phases of development.
Giuliani Capital Advisors LLC
Giuliani Capital Advisors LLC, an affiliate of Giuliani Partners LLC, is a boutique financial advisory and investment banking firm comprised of senior level professionals who provide a full range of capital raising, mergers and acquisitions, and financial and operational restructuring services.
ICON - A World-Class CRO
ICON Clinical Research is a full service clinical research organization providing a comprehensive range of clinical services in Phase I-IV clinical trials to the pharmaceutical, biotechnology and device industries world-wide. ICON offers integrated, global services spanning the entire clinical development continuum that are available on a stand-alone basis or as part of a comprehensive clinical program. Our clinical research teams have experience in a broad range of therapeutic areas including Cardiology, Dermatology, Gastroenterology, HIV/AIDS, Immunology/Inflammation, Infectious Diseases, Neurology, Oncology, Pain Management, Psychiatry, Pediatrics, Respiratory, Urology, Endocrinology, and metabolic diseases. http://www.iconplc.com
iGate Clinical Research International
iGATE Clinical Research was one of the first clinical research organizations to establish operations in India. In its 10 years of business, the firm has provided clinical operations/monitoring, data management/biostatistics, and CAP-accredited central laboratory services for some 75 Phase I to IV clinical trials. Over 40 CQA audits by global biopharmaceutical companies have confirmed iGATE CR's record of GCP compliance. With the infrastructure and support of a $300 million NASDAQ-listed parent company, iGATE CR offers unsurpassed quality of service, responsiveness and cost-effectiveness in India. http://www.igatecr.com
Kendle is a leading global clinical research organization providing the full range of early- to late-stage clinical development services for the world's biopharmaceutical industry. Our focus is on innovative solutions that reduce cycle times for our customers and accelerate the delivery of life-enhancing products to market for the benefit of patients worldwide. As one of the fastest-growing global providers of Phase I-IV services, we offer experience spanning more than 100 countries, along with industry-leading patient access and retention capabilities and broad therapeutic expertise, to meet our customers' clinical development challenges. www.kendle.com
Kforce Clinical Research Staffing
Kforce Clinical Research, a division of Kforce Inc., provides a full range of outsourcing alternatives and traditional staffing services for the pharmaceutical, biopharmaceutical and biotech industries. Established in 1988, Kforce Clinical Research is an industry leader in hybrid solutions, including functional outsourcing and the regional monitoring alliance model. Our expertise includes clinical trial monitoring and management, project management, drug safety and surveillance, clinical data management, SAS™ programming, biostatistics, data entry and clinical application development.http://www.kforce.com
Manipal Acunova is India's No 1 Emerging CRO. We conduct Phase I – IV Clinical Research, PK/PD Studies, CDM & Bio-statistics, Central Lab Testing and Core Imaging. We deliver quality data at 30% less cost 30% faster. We are soon recruiting patients in Latin America and Europe.
Oracle is a leading strategic software solutions provider to the health sciences industry, helping pharmaceutical, biotechnology, medical device, and healthcare organizations become the most successful in the world by offering the most innovative products and services that deliver the most compelling customer and shareholder value. Oracle's comprehensive industry solutions include clinical trial management and analysis, electronic data capture, adverse event reporting and pharmacovigilance, and healthcare interoperability. Oracle partners with health sciences industry leaders – including 20 of the top 20 life sciences companies and 14 of the top 14 Fortune Global 500 healthcare organizations – to prevent and cure disease, enhance quality of life, and accelerate insights for better health.
PRA 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.
Quest Diagnostics Clinical Trials consists of 600 employees dedicated to
central laboratory services for Phase II - IV clinical trials. Laboratories
are located in the United States, United Kingdom and India. Additionally,
Clinical Trials operates a project management office in Wavre, Belgium and
affiliate laboratories in Singapore, Melbourne and Shanghai.
Reliance Life Sciences
Reliance Clinical Research Services (RCRS) is a full-service CRO headquartered in Newtown, PA, with core facilities in Mumbai and Bangalore, India. With an organization of over 275 professionals, our services cover the areas of Pre-Clinical, Phase I (including bioequivalence studies), Phases II, III, and IV, Biometrics, Regulatory Affairs, Pharmacovigilence, and Bioanalytical, Diagnostic and Molecular Lab capabilities. The majority of our current clients are US or EU based; we have also successfully completed projects for companies in India, Israel and Japan. For further information, please refer to our website, www.relclin.com.
ResearchPoint is a global contract research organization providing all phases of drug and device development services to the pharmaceutical and biotech industries. With expertise spanning all major therapeutic areas, ResearchPoint delivers senior leadership to every project, resulting in creative problem solving, flexibility and superior customer service. Headquartered in Austin, Texas, ResearchPoint is able to offer a global reach through its membership in ResearchPoint Global, a worldwide partnership comprised of CRO's and technology service providers with local and regional expertise in 60 countries around the globe. http://www.researchpoint.com
Tata Consultancy Services (TCS)
Tata 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.
United BioSource Corporation
United BioSource Corporation delivers evidence-based solutions to optimize the medical and commercial potential of pharmaceuticals, biotechnology, medical devices, and diagnostics. We help provide scientific evidence to demonstrate product effectiveness and safety, minimize risk, and document economic value. Our capabilities include design and implementation of clinical studies, registries, and post-marketing surveillance; outcomes research and health economics studies; safety and risk minimization consulting; reimbursement planning and strategy; and investigator training and development.http://www.unitedbiosource.com