What does PRWW mean in NASDAQ SYMBOLS

Premier Research Worldwide (PRWW) is a full-service clinical research and development organization that provides comprehensive solutions to clients in the pharmaceutical, biotechnology, medical device, academic and government sectors. PRWW offers an innovative approach to help customers create and develop life-changing therapies while helping them maximize their return on investment.

PRWW provides a wide range of services from start to finish, including clinical strategy, trial execution and site management; protocol design; project management; data management; biostatistics; medical writing; eClinical solutions; regulatory affairs consulting; market access solutions; pharmacovigilance and quality assurance.

Any organization in the fields of pharmaceuticals, biotechnology, medical devices, academia or government can benefit from PRWW's customized solutions and tailored approach to suit their specific needs.

Through strategic planning and effective execution of clinical studies which are designed using cost effective approaches such as adaptive trial designs and multi-regional study sites, PRWW helps clients reduce their overall cost of drug development while maintaining high standards for safety and data integrity.

Yes! Our expertise spans five continents with over 18 year’s experience conducting trials worldwide in more than 70 countries. We have extensive experience with country-specific regulatory compliance requirements across Europe, Japan, Latin America and Asia Pacific regions.

Yes we do! We provide world-class Investigator Training Programs to ensure that our investigators understand the protocols they are working on and are familiar with all applicable GCP regulations at both national & international levels so that they can be fully prepared when conducting clinical trials.

At PRWW,we specialize in many aspects of drug discovery & development including Product Development & Regulatory Affairs Support Services such as Chemistry Manufacturing Controls (CMC), Medical Writing Services, Pharmacovigilance, Clinical Data Management so our clients have access to a full range of services that helps them bring new treatments to patients sooner.

Yes we do! We understand how crucial it is for companies to get timely regulatory approvals so our process leverages technology to help speed up the timeline without compromising accuracy or quality standards. Our expertise also extends into pre-submission preparation services such as document assembly & document publishing assistance so that our clients have successful outcomes when submitting materials into various markets around the globe.