Where do you start with technology solutions in your clinical trial? The many stages of study design are complex. Add to that the countless vendors ready to support the various aspects of study execution, and it starts to get confusing and hard to know where to begin.

It’s easy to be dazzled by that latest new technology or to slide into the rut of forcing your trial into the limits of the system your team already knows. Both of these easy options can result in inflated costs or compromised quality.

WHY IS TECHNOLOGY-AGNOSTIC A BETTER APPROACH?

We focus on the big-picture strategy for your specific needs. At Worldwide Clinical Trials, we respect that you may have preferred technology solutions, and we are prepared to work with any system that enables your success. If you are unfamiliar with technology, or if you are open to our recommendations, we can assess your trial’s unique parameters and identify those vendors best suited to the demands of your program. We don’t provide a one-size-fits-all solution. In every aspect of your trial, we are available to provide the best recommendations fit for your purposes.

WE IMPLEMENT SOLUTIONS THAT FIT YOUR PRIORITIES

Along with focusing on your strategy, we also work with your priorities in terms of budget, scope, and schedule. Worldwide can honestly assess how much time and money is required to reach your goal and work to build solutions that match your ambitions.

WE HAVE RELATIONSHIPS IN PLACE TO TAKE THE GUESSWORK OUT

Your focus is moving your drug development program forward. As part of your partnership with a full-service CRO like Worldwide, we expect you to rely on us for the technology. We’ve built relationships with the best-of-breed tech providers and can offer you the best platform fit for your purpose. Take the guesswork out of technology, and trust Worldwide for all your program needs.

READY TO LEARN MORE? CONTACT WORLDWIDE NOW.

LEARN MORE ABOUT WORLDWIDE’S PARTNERSHIPS
WITH TECHNOLOGY PROVIDERS

WEBINAR:
HOW TECHNOLOGY IMPROVES OPERATIONAL EFFICIENCY AT
WORLDWIDE
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WORLDWIDE
CLINICAL TRIALS AND MEDIDATA STREAMLINE
CLINICAL SITE REIMBURSEMENTS
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WORLDWIDE CLINICAL TRIALS AND DEEP LENS PARTNER TO ACCELERATE RECRUITMENT AND DEVELOPMENT TIMELINES
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WORLDWIDE CLINICAL TRIALS IMPLEMENTS CLINSPARK ESOURCE PLATFORM
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OUT OF THE BOX

Worldwide Delivers Best-of-Breed Utilization and Partnerships

PAYMENT SOLUTIONS
Get your sites and patients paid securely, accurately, and on time. Do you need a solution that manages your budget and forecasting, that can talk to other systems in your trial workflow? We can help you identify the solution that best suits your payment and budget management needs.
TALENT AND
PERFORMANCE
MANAGEMENT
We’ll help you determine which solution can best align your workforce with the goals and obligations of your project. Whether you need to provide onboarding, ongoing training, performance appraisals, or additional resources, there is a solution for your needs.
PATIENT AND
SITE RECRUITMENT/
RETENTION
The key to a successful trial is getting a group of study subjects. From recruiting to compliance monitoring, we help you find the solution that builds the patient group your study requires.
VIRTUAL, REMOTE
MONITORING AND
WEARABLE
TECHNOLOGIES
Remote reporting technologies run from fitness trackers to medical monitoring devices. We’ll identify the solutions to get you data that passes regulatory scrutiny on easy-to-use devices.
BIOANALYTICAL
AND CENTRAL
LAB
It’s important to understand what measurements will be needed, and what technology has been proven and accepted by regulatory agencies. We can identify the vendor best equipped to manage your lab processes.
GLOBAL CLINICAL
SUPPLY AND
DEPOT
With data quality and patient safety so critical, the costs of keeping your supply chain running can have high variability. We can help you find the solution that best fits your supply needs and timeline considerations.
CLINICAL TRIAL
MANAGEMENT,
PHARMACO-
VIGILANCE AND
GENERAL
INFRASTRUCTURE
We can help you find the platform that covers your bases for trial oversight, patient compliance and safety, site operations, and any other functions needed, without unnecessary bells and whistles.
ELECTRONIC CLINICAL
OUTCOME
ASSESSMENTS
(eCOA)
Think of eCOA as the treasure chest of the clinical trial, the system that collects that valuable patient data, ensuring its accuracy and timeliness, and then presenting it in informative formats for your stakeholders. We’ll find you the eCOA vendor that gives you accurate data, on time.
IRT
(IVRS/IWRS)
To what extent will telephone or web reporting systems serve your trial, how will they integrate with your trial management system, and which system can your patients most readily work with? We can go through these questions with you to identify the best IRT fit for you.
eTMF
As you document the life cycle of your clinical trial, you’ll need to determine what types of data will have to be managed within your TMF system. We’ll identify the system that can get your documentation prepared for regulatory inspection.
DATA COMPLIANCE, CAPTURE,
MANAGEMENT, REPORTING,
AND VISUALIZATION
We’ll identify the solution that can get your project’s stakeholders the information they need, in a time frame that aligns with your requirements.
CLINICAL,
REGULATORY AND
QUALITY SYSTEMS
What are the vulnerabilities in your trial, those areas where you might need support in maintaining regulatory or safety standards? We’ll help you find which system can address your trial’s pain points and help you mitigate risk, while maintaining regulatory compliance and achieving quality data.