Clinical Research Organization
At Research Drive, we are not just a CRO; we are an independent partner in advancing healthcare through exceptional support in clinical research.
Your Partner in Clinical Research
At Research Drive, we are specialized in providing tailored Clinical Research Organization (CRO) services to support your clinical trials from concept to completion.
With expertise in regulatory submissions, site management, monitoring, project management, and Trial Master File (TMF) management, we ensure seamless trial execution with a focus on compliance, quality, and efficiency.
Our team of dedicated professionals is committed to guiding you through every phase of your clinical trial, offering customized solutions to meet your unique needs. Whether you are navigating complex regulatory requirements or seeking robust site and data management, we are here to deliver results with precision and excellence.
Our Services
Let’s collaborate to bring your innovative treatments to life.
Regulatory Submissions
Regulatory submissions and approvals are a critical part of the clinical trial process.
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Monitoring and Site Management
Our expert Clinical Research Associates (CRAs) are committed to maintaining the highest standards of data integrity and patient safety across all phases of clinical trials.
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Project Management
The Project Managers at Research Drive are experts in the discipline of planning, organizing, and managing resources to ensure the successful completion of a client’s clinical trial project.
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On-site study management
At Research Drive, we go beyond monitoring visits alone. We understand that sites face limited resources, staffing challenges, and tight timelines.
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Trial Master File Management
The Trial Master File (TMF) serves as backbone of your trial’s documentation, providing a comprehensive record of all essential documents.
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CRO Oversight Services
Effective CRO oversight is more than regulatory obligation, it is a strategic opportunity to enhance the quality, efficiency, and success of your clinical trial.
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Regulatory inspection and Audit readiness on site
Preparing for audits from the Sponsor/CRO or inspections by authorities such as the FDA, EMA, or local Health Authorities require thorough preparation, accurate documentation, and full compliance with ICH-GCP and protocol standards.
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Quality Assurance and Auditing
At Research Drive, we understand the critical importance of maintaining the highest standards in clinical research.
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Veterinary Trials
Research Drive brings experience in conducting veterinary clinical trials, offering specialized services tailored to the unique needs of veterinary research.
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Read our client testimonials about their experiences on working together with Research Drive.