Break the data barrier now
Complying with regulatory requirements is vital. Competition is fierce. And costs are spiraling. As if that weren’t enough, many clinical software solutions can't keep up with the deluge of data you need. The truth is, your current system could be slowing your time to market.
PAREXEL® Informatics aims to put an end to fragmentation, redundancies and difficulties in the management of clinical and operational data – from study planning to regulatory submission and management. And everything in between.
Our open eClinical solution, Perceptive MyTrials®, features a collaborative design environment to accelerate study set-up. It also provides a single point of access and common user experience across applications. And it works with the systems you have now. Perceptive MyTrials will speed your trials through:
Opinions may vary on the details, but everyone agrees speeding up clinical trials is a good thing. What’s your point of view?
How long does it take to configure your clinical trial systems and implement the study protocol?
Are you able to work interactively with your CRO on study design?
Have you had to rework study designs and experienced delays in study start-up?
What causes the biggest delay during your clinical trial processes?
Do you and your sites have quick and easy access to work with relevant data?
How do your study teams access trial information?
Learn more about how PAREXEL Informatics solutions speed clinical trials on their way.
EDC – Get a handle on Clinical Data Management
Technology and data services to accelerate your drug development process
ePRO (Data sheet)
How will you ensure regulators and payors accept your PRO-based submission?
ClinPhone® RTSM (Data sheet)
Do you know where your supplies need to be?