Skip links



Consolidating clinical trial management in one dashboard

Schedule a Free Demo with us Today!

Technologies We Used To Build The Next Big Thing

Built for Simplicity

Connecting Emails

No need for time-consuming questions, emails, or phone calls, to check the progress of trials.

Speed up the trial cycle

Reduce pointless holdups and advance clinical trial schedules for prompt results.

Automated Notifications

The automated alerts let stakeholders stay up-to-date throughout the trial process.

Detailed Reporting

Lets you be thorough with trial, site, or organization reporting


Efficient Task Tracking

Let you track the study initiation process seamlessly.

Dashboard and Reports

Track trial possibilities, timing, and performance with ease.

Scalability and Reach

Adjust your design through a wide range of theme options in the Customizer.

Accommodate diverse pre-clinical trial scenarios.

Learn more

Robust scaling of pre-clinical trial activities

Learn more

Dynamic growth strategies

Learn more

Adaptable operational approaches

Learn more

Increase the scope and reach of your pre-clinical trials

Learn more

Adjust to changing study parameters

Learn more
Streamlined Workflows

Automate repetitive tasks and streamline administrative processes, allowing researchers to focus on critical scientific work.

Time Savings

Save valuable time by reducing manual data entry, protocol management, and document handling.

Faster Study Initiation

Accelerate the study startup phase by efficiently managing protocols, approvals, and participant data.

Secure Data Handling

Protect sensitive trial data with robust encryption and access control measures.

Patient Confidentiality

Safeguard patient and participant data to maintain trust and comply with data privacy regulations.

All the tools you need
to manage Clinical Trials

All the tools you need

to manage Clinical Trials

Generate reliable and accurate reports, ensuring data integrity and compliance with regulatory standards.

Ensure adherence to regulatory requirements, reducing the risk of non-compliance issues and penalties.

Maintain a comprehensive audit trail for transparency and accountability, critical for audits and inspections.

Need help?

FreshDesk Support

Call us to get your questions about Syncora answered

Talk to Our Experts

Have more queries about Syncora? Schedule a call with our experts Need assistance with Syncora? Schedule a call with our experts

Schedule a Demo

Experience more features of Syncora by scheduling a demo with us

Customizable per your needs

Syncora Allows You
To Customize

Never lose track of your data, with Syncora pre-clinical Trial management at your fingertips.

Track Data <br>Manage

Track Data

Timelines <br>Regulatory




Have a question?
Let’s talk about it

Syncora automates time-consuming administrative tasks, freeing up researchers to focus on their scientific work leading to faster study initiation and efficient workflows.
Syncora complies with regulatory requirements, It includes features like audit trails and access controls to meet these standards.
Syncora facilitates centralized communication tools, enabling research teams, sponsors, and sites to share information and updates.
Syncora includes advanced data analytics tools that allow you to derive valuable insights from research data.
One-stop hub for clinical trials

Why Choose Syncora

Make your clinical trials easier with Syncora.

Other pre-ctms software
Moderate learning curve

Basic planning features

Limited revision tracking

Limited site oversight

Limited data entry

Basic reporting features

User-friendly interface

Efficient data tracking

Comprehensive data storage

Real-time site monitoring

Automated compliance checks

Advanced analytics tools

Still have a question? Browse documentation or submit a ticket.

Let’s schedule

a live demo

Reach out to us today to schedule a demonstration and watch Syncora live-action.

Need better data?
Synocora will be your guide to creating, streamlining, and propelling your clinical trial start-ups.