General Information

PRA International is one of the world’s leading global clinical research organizations (CROs). The company provides global clinical drug development services on a contract basis to pharmaceutical and biotechnology companies. PRA is headquartered in Raleigh, North Carolina, and has over 3,000 employees working from 27 offices in North America, Europe, Africa, South America, Australia and Asia.

Customers choose to work with PRA for a variety of reasons. Foremost among these are our reliability in delivering consistent high quality services, full range of clinical development services, global coverage, therapeutic expertise in oncology, CNS, allergy/respiratory and cardiovascular, and strong data management capabilities.

PRA Locations

PRA's corporate headquarters are located in Raleigh, NC, USA. Clinical trials and related services are conducted from offices located in:

• North America
  • Austin, Texas, USA
  • Charlottesville, Virginia, USA
  • Horsham, Pennsylvania, USA
  • Lenexa, Kansas, USA
  • San Diego, California, USA
  • Victoria, British Columbia, Canada
• Europe
  • Paris, France
  • Mannheim, Germany
  • Budapest, Hungary
  • Warsaw, Poland
  • Moscow, Russia
  • Madrid, Spain
  • Mechelen, Belgium
  • Reading, England, UK
  • Swansea, Wales, UK
  • Assen, The Netherlands
  • Groningen, The Netherlands
  • Zuidlaren, The Netherlands
• Africa
  • Cape Town, South Africa
  • Johannesburg, South Africa
• Asia
  • Taipei, Taiwan
  • Mumbai, India
  • Pune, India
• Australia
  • Sydney, Australia
• South America
  • São Paulo, Brazil
  • Buenos Aires, Argentina

PRA Mission

As one of the top five global clinical development organizations in the world, PRA is positioned to help pharmaceutical, biotechnology and medical device firms bring modern medical products to the market as quickly as possible. With years of diverse experience and highly refined management skills, PRA provides end-to-end clinical development solutions, including: comprehensive product development services; design, implementation and analysis of Phase I-IV clinical study projects; outsourced clinical operations; and specialized services such as electronic regulatory submissions.

Our far-reaching operations are tied together by a robust information technology network that supports reliable global access and efficient management of vital real-time and historical clinical data. PRA has established a reputation for outstanding customer service, quality work products and reliable performance.

PRA invests heavily in senior medical and scientific staff, staff development programs, well-designed facilities, information technology, integrated information systems, process engineering, customer account management, and quality assurance systems. PRA operates with the same standard operating procedures (SOPs), systems and business practices worldwide to conduct clinical trials according to the same high standards at every location.

PRA Services

PRA International offers a broad array of services encompassing the entire spectrum of clinical development programs, from filing of Investigational New Drug (IND) and similar applications to product registration and post-marketing surveillance. PRA’s global clinical development services include:

• Phase I - IV study management
• Feasibility and protocol design
• Clinical development strategies
• Bioanalysis, including biomarkers
• Data Monitoring Committee management and support
• Traditional and electronic data capture (EDC)
• Prospective and retrospective database integration
• Regulatory approval strategies and electronic submissions

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