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At Cloudbyz, we are deeply committed to driving innovation in the medical device industry. We understand the intricacies and complexities of conducting clinical trials, and our solutions are designed to simplify the process, thereby enhancing efficiency and promoting faster time-to-market for breakthrough medical devices.

CRO

Our Solutions

Our unified clinical trial management solutions offer end-to-end management for clinical trials within the medical device industry. By unifying the end-to-end clinical trials management process, our platform acts as a comprehensive hub for patient recruitment, trial operations management, budgets and financials, study start-up, data capture, safety, and reporting.

All-in-One Clinical Trials System
CTMS

Seamless End-to-End Clinical Trial Operations

Increased Collaboration
CTBM

Real-time Visibility on Budgets and Payments

Advanced Analytics & Reporting
eTMF

Improve Trial Management with Real-time Collaboration

Compliance and Security
EDC

Accelerate study build and data capture

Improved Data Quality
RTSM

Integrated randomization and trial supply management

Configurable and Scalable
Safety

Unified Safety adjudication and reporting

Key aspects of our solution include

All-in-One Clinical Trials System
Unified

One system for all your needs. From trial design to closing, from regulatory compliance to data management, we have you covered.

Increased Collaboration
User-friendly

Our platform is designed with user experience in mind, ensuring your team can easily navigate and make the most of its features.

Advanced Analytics & Reporting
Scalable

Whether you're a startup or a multinational corporation, our system can adapt to your needs, facilitating growth while maintaining consistent performance.

Compliance and Security
Compliant

With a keen focus on regulatory compliance, our solutions help ensure that your trials are conducted ethically and within the boundaries of global and regional regulations.

Benefits

All-in-One Clinical Trials System
Increased efficiency

Streamline operations, reduce redundancy, and enhance productivity by managing all your trial activities from one central hub.

Increased Collaboration
Improved data integrity

Enjoy accurate, reliable data that can be accessed in real-time, facilitating better decision-making.

Advanced Analytics & Reporting
Reduced time-to-market

By optimizing your clinical trials process, you can shorten your development timeline, getting your device to market quicker.

Compliance and Security
Greater compliance

Stay ahead of regulations with our integrated compliance modules, designed to help you maintain ethical and regulatory standards.

Contact Us

ISO 270001
21CFR
ICH
Hippa
ISO 9001
GDPR