PRA International, a prominent global contract research organization, specializes in providing outsourced clinical development and data solution services to the pharmaceutical and biotechnology industries. The company operates through two main segments: Clinical Research and Data Solutions. The Clinical Research segment encompasses a wide range of services, including clinical trial management, regulatory affairs, biostatistics, and quality assurance, as well as early development services for Phase I and Phase IIa studies. The Data Solutions segment offers various analytical and consulting services, enabling clients to access and interpret vital data through technology-enabled products. With over 17,000 employees and operations in more than 90 offices worldwide, PRA International has played a crucial role in advancing drug development, having participated in over 3,800 clinical trials and supporting pivotal studies that led to the regulatory approval of numerous products. The organization has also partnered with The Leukemia & Lymphoma Society to develop treatments for childhood leukemia. Founded in 1976 and headquartered in Raleigh, North Carolina, PRA International is recognized for its commitment to excellence in clinical research.
Care Innovations specializes in technology-based healthcare management services that facilitate connections between individuals and caregivers. The company focuses on collecting, aggregating, and analyzing data to deliver actionable insights that bridge the gap between healthcare providers, payers, caregivers, and consumers. By enabling a seamless care continuum within the home, Care Innovations supports individuals in maintaining their independence while also aiming to reduce overall healthcare costs.
Parallel 6 is a software as a service (SaaS) provider specializing in mobile enrollment and engagement solutions tailored for clinical research and public sector organizations. The company has developed a mobile platform that facilitates the management and participation in clinical trials. This platform enables the digital enrollment, engagement, and management of patients through mobile endpoints, allowing for real-time data access and reporting from clinical sites and patients. By seamlessly integrating into patients' daily lives, Parallel 6 enhances the efficiency of clinical research while providing sponsors with valuable insights and data from anywhere in the world.
Symphony Health Solutions offers data, analytics, applications, and consulting services tailored for life sciences companies. Based in Horsham, Pennsylvania, with an additional office in Phoenix, Arizona, the company provides a wide range of services including market sizing, sales force analytics, message delivery effectiveness, patient and prescriber analytics, and revenue forecasting. By delivering comprehensive data and insights, Symphony Health Solutions helps clients navigate complex healthcare dynamics, enabling them to make informed decisions that enhance brand performance and optimize sales strategies. Their extensive data resources capture real-world interactions among physicians, payers, and patients, providing a holistic view of the market lifecycle, from predictive analysis to reimbursement strategies. As a subsidiary of Pharmaceutical Research Associates, Inc., Symphony Health Solutions remains focused on empowering biopharmaceutical manufacturers, healthcare providers, and payers to improve their operational effectiveness in an evolving healthcare landscape.
Nextrials, Inc. specializes in providing web-based software solutions for the clinical research industry, focusing on electronic data capture and clinical trial data management. The company's primary product, Prism, is an integrated solution that offers standard data management functions alongside additional tools for effective clinical trial data collection and management. Nextrials also offers E2E, a tool that enhances data collection by directly extracting clinical data from electronic health records, thereby streamlining the process and improving data quality. The company caters to biopharmaceutical and medical device companies both in the United States and internationally. Founded in 1999 and headquartered in San Ramon, California, Nextrials operates as a subsidiary of PRA Health Sciences, Inc.
Value Health Solutions Inc. is a subsidiary of PRA Health Sciences, specializing in integrated clinical trial management solutions. The company focuses on enhancing health outcomes for patients by offering a range of services, including app development, business process reengineering, and maintenance services. Utilizing offshore centers, Value Health Solutions converts traditional paper-based processes and costly digital solutions into automated, efficient digital assets through its productized offerings. This approach aims to streamline clinical trials and improve overall patient care.
CRI Lifetree operates as a specialized research organization. The Company focuses on the conduct and design of early stage endocrinology and infectious disease research products and services. CRI Lifetree provides clinical research throughout the United States.
ReSearch Pharmaceutical Services, Inc. is a provider of integrated clinical development solutions for the bio-pharmaceutical industry. The company offers a range of services, including clinical trial project management, site management, study monitoring, patient enrollment, data collection and management, statistical analysis, report writing, quality assurance, and regulatory and medical affairs support. These services assist clients in the design, initiation, and management of clinical trials across various therapeutic areas, such as cardiovascular, oncology, infectious diseases, neurology, and pediatrics. Founded in 1994, ReSearch Pharmaceutical Services is headquartered in Fort Washington, Pennsylvania, and operates in North America, Latin America, Europe, and Asia.
ClinStar, LLC, a clinical research organization, provides clinical development services to pharmaceutical and biotechnology industries in the Russian Federation and Eastern Europe. It manages phase I-IV clinical research trials in the Russian Federation, Ukraine, Belarus, and the Baltic States. The company offers feasibility, regulatory submissions, clinical development, medical monitoring, and logistics services; and GCP audit services, including investigator site audits, trial master file audits, vendor quality systems audits, central laboratory audits, drug depot audits, and preparation for regulatory inspections.
Kinship Technologies is a global provider of innovative software products and services aimed at enhancing and streamlining the drug development process for the pharmaceutical, biotechnology, contract research organization (CRO), and medical device industries. The company specializes in its EXACT software, which facilitates data extraction, transformation, statistical reporting, and electronic publishing, thereby simplifying the creation of industry-standard reporting deliverables. In addition to its software solutions, Kinship Technologies offers a range of services, including biostatistical analysis, CDISC consultancy, and custom programming and reporting, all designed to optimize and expedite the clinical development process.
Pharma Bio-Research Group
Acquisition in 2006
Pharma Bio-Research Group B.V. provides contract research, clinical, bio analytical and biometrical/statistical, and support services to the pharmaceutical and biotechnology industries. The company offers services for phase I/IIA clinical research, as well as specializes in single and multiple dose tolerance studies, pharmacokinetic/pharmacodynamic and mass balance/ADME studies.
Sterling Synergy Systems
Acquisition in 2006
Sterling Synergy Systems Private Limited operates as a contract research organization in India. The company provides a platform to design, conduct, and monitor clinical development services for Phase II - IV trials. It also offers project management services. Sterling Synergy Systems has facilities in Lenexa, Kansas; Victoria, British Columbia; and Swansea, Wales, as well as a data management center in Pune, India.
GMG BioBusiness, Ltd., based in London, United Kingdom, specializes in regulatory and product development consulting services for the pharmaceutical industry. The company assists clients with various aspects of the drug development process, including centralized and mutual recognition filings, labeling preparation, clinical trial applications, and accelerated submissions and approvals. GMG BioBusiness focuses on therapeutic areas such as oncology, inflammatory conditions, and orphan drugs, providing strategic support and regulatory resources to aid companies through clinical development, registration, and market launch.
Regulatory/Clinical Consultants, Inc. is a contract research organization that provides consultancy and support services to the pharmaceutical and biotechnology sectors. The company specializes in regulatory affairs, offering services such as regulatory consulting, quality assurance, auditing, medical writing, clinical study monitoring, and electronic regulatory submissions. Additionally, it focuses on health economics and outcomes research to facilitate the regulatory approval process globally. By delivering tailored solutions, Regulatory/Clinical Consultants aims to assist clients in navigating the complexities of regulatory requirements and achieving compliance in their product development efforts.
ClinCare Consulting
Acquisition in 2003
ClinCare's principal service offering is clinical trial project management and investigational site monitoring. Their therapeutic experience includes cardiovascular, central nervous system, oncology, and rheumatology, as well as considerable experience with device trials.
CroMedica International Inc. is a clinical research organization that provides drug development strategy and study design, clinical trial management, phase 1/2a research facilities, and clinical supplies management services. Its clinical trial management services include drug development strategy, protocol design, case report form preparation, regulatory submissions, clinical trial supplies management, investigator meetings and site training, project management, medical and clinical monitoring, pharmacovigilance, and data management and analysis.
International Medical Technical Consultants
Acquisition in 1997
International Medical Technical Consultants, Inc. is a contract research organization which engages in clinical trials including asthma and allergy studies. The company assists pharmaceuticals companies in drug development activities for curing asthma and allergy. T
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