Streamlined Clinical Trial Activation

Efficient Contract and Budget Management for Seamless Trial Execution

With a focused commitment to efficiency and excellence, our streamlined activation process significantly reduces the average start-up time for clinical trials to just 61 days. This rapid mobilization enhances patient enrollment and aligns seamlessly with your critical timelines, ensuring no time is lost.

Key Advantages at a Glance

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Average Study Start-Up Time

Our expert coordination expedites site activation, allowing your study to commence swiftly.

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Site Activation Success Rate

We pride ourselves on our high success rate in activating sites, thanks to our effective and clear onboarding processes.

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Training Completion Rate

Comprehensive training of our team ensures strict adherence to protocols, supporting flawless trial execution.

Comprehensive Contract and Budget Management

We excel in contract and budget negotiations, prioritizing transparency and strategic financial alignment tailored to each trial's needs. Our approach ensures not only cost-efficiency but also strict adherence to timelines and project scopes.

Key Features of Our Approach

1

Customized Agreements:

We tailor contracts to the specific demands of each trial, ensuring compliance and project alignment.

2

 Risk Management:

We proactively manage financial and operational risks through strategic planning.

3

Budget Clarity:

We maintain complete transparency in budgeting, preventing any hidden costs

4

Efficient Use of Resources:

Every dollar is strategically allocated to maximize trial efficiency and outcomes.

Timeliness & Compliance Targets

1

Data Entry

Within 22 hours

2

Query Resolution

Within 48 hours

3

SAE Reporting (IRB & Sponsor):

Within 6 hours after the site becomes aware of the SAE

4

Regulatory Submissions to IRB:

Within 24 hours after sponsor approval

5

Essential Documents Completion:

within 5 days of receiving the regulatory package

Why Choose Us?

Centralized Quality & Regulatory Support

Uniform processes across all trial sites ensure faster turnarounds while meeting rigorous quality and regulatory standards.

Dedicated Support Teams

Our regulatory and clinical data management teams work together to maintain data integrity and compliance, which facilitates smooth FDA audits and regulatory submissions.

Partner with us for expedited clinical trial activation that adheres to the highest standards of quality and regulatory compliance, ensuring your projects proceed on schedule and with optimal outcomes.