SPEED

GET TO FIRST PATIENT FASTER

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:

  • Trial design, implementation and optimization
  • Randomization and supply management
  • Data collection and management
  • Rapid integration using industry standards
  • Data retrieval, verification, reporting and analysis

YOUR PEERS HAVE SPOKEN - IT’S YOUR TURN

Opinions may vary on the details, but everyone agrees speeding up clinical trials is a good thing. What’s your point of view?

See how long it takes your peers to configure clinical trial systems and implement study protocols.

3 Keys to Operational Excellence for Clinical Trials

 

Are you able to work interactively with your CRO on study design?

Are you able to work interactively with your CRO on study design?

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Have you had to rework study designs and experienced delays in study start-up?

Have you had to rework study designs and experienced delays in study start-up?

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What causes the biggest delay during your clinical trial processes?

What causes the biggest delay during your clinical trial processes?

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Do you and your sites have quick and easy access to work with relevant data?

Do you and your sites have quick and easy access to work with relevant data?

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How do your study teams access trial information?

How do your study teams access trial information?

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