PRA Health Sciences

Care Innovations is a provider of technology-driven healthcare management services focused on connecting individuals with caregivers. The company specializes in collecting, aggregating, and analyzing healthcare data to deliver actionable insights that integrate the roles of providers, payers, caregivers, and consumers. By facilitating a seamless care continuum within the home, Care Innovations aims to empower individuals to live independently while also contributing to the reduction of healthcare costs.

Parallel 6 is a 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 innovative platform allows for the digital enrollment and engagement of patients, utilizing mobile endpoints to connect with and manage patients globally. By seamlessly integrating into patients' daily lives, the platform enables sponsors to access real-time data and reports from clinical sites and patients, all within a unified system.

Symphony Health Solutions is a provider of comprehensive data, analytics, and consulting services tailored for the life sciences industry. Based in Horsham, Pennsylvania, with an additional office in Phoenix, Arizona, the company specializes in delivering insights that address the complexities of the healthcare market. Its services encompass a wide range of analytical capabilities, including segmentation analysis, sales force analytics, and forecasting, which empower clients to make informed decisions regarding brand performance and market strategies. Symphony Health's integrated data solutions capture real-world dynamics, enabling stakeholders such as biopharmaceutical manufacturers, healthcare providers, and payers to enhance their operational effectiveness and adapt to the evolving healthcare landscape. As a subsidiary of Pharmaceutical Research Associates, Inc., Symphony Health leverages its unique data and research capabilities to provide critical insights throughout the entire market lifecycle, from patient influence to payer reimbursement.

Nextrials, Inc. is a provider of web-based software solutions tailored for the clinical research industry. Established in 1999 and headquartered in San Ramon, California, the company specializes in electronic data capture and clinical trial data management. Its flagship product, Prism, is an integrated solution that offers essential data management functions along with additional tools for effective clinical trial data collection and management. Nextrials also develops E2E, a data collection tool that interfaces directly with electronic health records (EHR) systems to enhance the efficiency and quality of data collection. Serving biopharmaceutical and medical device companies both in the United States and internationally, Nextrials aims to help clinical researchers maximize the value of trial data while reducing development costs and accelerating time to market. As of 2016, Nextrials operates as a subsidiary of PRA Health Sciences, Inc.

Value Health Solutions Inc. is a prominent provider of integrated clinical trial management services, focused on improving health outcomes for patients. As a subsidiary of PRA Health Sciences, the company specializes in transforming traditional paper-based processes into automated, digital solutions through app development and business process reengineering. By utilizing offshore centers for technology, Value Health Solutions aims to create efficient and cost-effective clinical trial management systems that enhance the overall effectiveness of clinical research.

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., founded in 1994 and headquartered in Fort Washington, Pennsylvania, offers integrated clinical development solutions to the bio-pharmaceutical industry. The company provides a comprehensive range of services that include project management, site management, study monitoring, patient enrollment, data collection and management, statistical analysis, report writing, quality assurance, and regulatory and medical affairs. These services facilitate the design, initiation, and management of clinical trial programs across various therapeutic areas, such as cardiovascular, oncology, infectious diseases, neurology, allergy/immunology, endocrinology/metabolism, gastroenterology, obstetrics/gynecology, orthopedics, pediatrics, and psychiatry. ReSearch Pharmaceutical Services operates across North America, Latin America, Europe, and Asia, making it a significant player in the global clinical development landscape.

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 leader in providing innovative software products and services designed to enhance and expedite the drug development process for the pharmaceutical, biotechnology, contract research organization (CRO), and medical device industries. The company specializes in developing solutions that facilitate integration and automation, thereby streamlining various phases from data source management to regulatory submission. Its flagship software, EXACT, enables users to create reusable programs for data extraction, transformation, statistical reporting, and electronic publishing, automating the generation of standardized reporting deliverables such as CDISC SDTM and ADaM. Additionally, Kinship Technologies offers a range of services including biostatistical analysis, CDISC consultancy, and customized programming and reporting, all aimed at improving efficiency and compliance in clinical development.

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 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.

Regulatory/Clinical Consultants, Inc. is a contract research organization dedicated to supporting the pharmaceutical and biotechnology sectors in achieving regulatory approval on a global scale. The company provides a comprehensive range of consultancy services, including regulatory affairs, quality assurance, auditing, compliance, medical writing, and clinical study monitoring. Additionally, it specializes in electronic regulatory submissions and health economics and outcomes research, ensuring that clients receive tailored solutions to navigate complex regulatory environments effectively. Through its expertise, Regulatory/Clinical Consultants aims to facilitate the development and approval processes for innovative medical products.

GMG BioBusiness, Ltd. is a consultancy firm based in London, United Kingdom, specializing in regulatory affairs and product development services for the pharmaceutical industry. The company assists clients with a range of activities, including centralized and mutual recognition filings, labeling preparation, and clinical trial applications. It also offers support for accelerated submissions and approvals, as well as due diligence and development strategies. GMG BioBusiness focuses on therapeutic areas such as oncology, inflammatory diseases, and orphan drugs, providing strategic guidance and regulatory resources to help clients navigate clinical development, registration processes, and market launches effectively.

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, 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