This market research report was developed based off of the responses of 301 industry professionals involved in outsourcing Phase II/III projects, and the service encounters they’ve had over the last 18 months. It includes information on respondent’s outsourcing philosophies and practices, their perceptions of and experiences with CROs involved in Phase II/III trials, CRO selection criteria, and their performance analysis of 41 different CROs.
Worldwide Clinical Trials employs more than 1,400 professionals around the world, with offices in North and South America, Eastern and Western Europe, Russia and Asia. One of the world’s leading, full-service contract research organizations (CROs), we partner with sponsors in the pharmaceutical and biotechnology industries to deliver fully integrated clinical development and bioanalytical services, extending from first-inhuman through phase IV studies. Grounded in medicine and science, Worldwide Clinical Trials enables sponsors to move from medical discovery into clinical development and commercialization, helping bring innovative solutions to market that deliver enhanced value and improve patient lives. Our employees are among the best in their fields – clinicians, scientists, operational and regulatory specialists who offer expertise across a range of therapeutic areas, including neuroscience, cardiovascular diseases, immune mediated inflammatory disorders (IMID), and rare diseases.
The number of blockbuster drugs and products launched by pharmaceutical, biotechnology and medical device industries continues to shrink.
All clinical trials collect regulatory documentation in order to receive authorization to conduct the trial at investigative sites. Trials require a Regulatory Binder and many keep separate Study Binders.
Our trained regulatory attorneys and compliance professionals provide actionable, effective solutions to complicated research scenarios and product development. Plus, we track and address the ever-changing legal and regulatory landscape to provide current, on-demand regulatory support & tailored directly to you.
The iMedNet Partner Program is designed to help CROs and consulting organizations improve efficiency, expand their service offerings, and win more business.
Trial Interactive is the all inclusive source for all of your clinical data management needs. In addition to hosting clinical trial solutions and electronic case site solutions, we also provide a full array of scanning and clinical document management services.
Worldwide Clinical Trials Bioanalytical Sciences has built its reputation on providing quality service with rapid turnaround at a competitive cost. With the most modern bioanalytical instrumentation and more than 1,500 methods, we are at the forefront of the industry in the development of bioanalytical methodology. We can develop a custom method for your compound(s) or transfer/modify your existing method.
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