Break the data barrier now
Recent statistics suggest the cost of bringing a drug to market could be as high as $5.8 billion1, with about 90% of it from clinical trials. Considering the exposure that expense creates, biopharmaceutical companies increase risk any time they don't put an expert on the job.
PAREXEL® Informatics puts best practice standards within reach for every clinical trial: our solutions are developed, operated and supported by experts with a proven track record. They're available to help customize and build your study design, develop randomization algorithms, implement trial supply management, and provide support to help your products navigate regulatory and development obstacles.
Opinions may vary on the details, but everyone agrees having experts help you set up and manage clinical trials is a good thing. What’s your point of view?
If you run into a problem, would you be more likely to?
Are you satisfied with your customer service during your clinical trials?
What is the most important factor you’d like to see addressed?
What causes the biggest delay during your clinical trial processes?
Learn more about how PAREXEL Informatics services reduce risk.