Clinical Data Management

Clinical Data Management (CDM)

At OrciTrials, we understand the pivotal role that accurate and efficient Clinical Data Management (CDM) plays in the success of clinical trials and research. Our comprehensive Clinical Data Management services are designed to meet the unique needs of pharmaceutical, biotechnology, and medical device companies, ensuring that your clinical data is managed, validated, and analyzed with precision.


We offer comprehensive Data Management Services tailored to meet your organization’s unique needs. Managing data efficiently is crucial for informed decision-making, regulatory compliance, and maintaining a competitive edge in today’s data-driven world.

Our Services

Data Collection and Capture:
We help you design and implement data collection processes that are intuitive, efficient, and compliant with industry standards. Our data capture solutions include electronic data capture (EDC) systems, paper-based solutions, and more.
Data Entry and Validation:
Our team ensures that all data entered into your clinical trial databases are accurate, complete, and compliant with regulatory guidelines. We perform thorough data validation to maintain data integrity.
Database Design and Build:
We create robust and secure databases for your clinical trials, optimizing them for data storage, retrieval, and reporting. Our databases are designed to facilitate data analysis and ensure data quality.
Query Management:
We proactively identify and resolve data discrepancies by managing queries efficiently. Our team communicates with investigators and site staff to address issues promptly, ensuring data accuracy and completeness.
Data Cleaning and Quality Control

OrciTrials employs a rigorous data cleaning process to eliminate inconsistencies, errors, and outliers. We perform data quality checks throughout the trial, guaranteeing reliable results.

Data Security and Compliance:
Your data’s security and compliance are our top priorities. We adhere to all regulatory requirements and use cutting-edge technology to maintain data confidentiality and integrity.
Statistical Analysis and Reporting:

OrciTrials leverages the latest technology to streamline data management processes. Our EDC and clinical trial management system (CTMS) integration enhances data flow, reducing errors and inefficiencies.

Why Choose Orcitrials for Clinical Data Management?

Experience:

With years of experience in clinical data management, OrciTrials has a proven track record of successful collaborations with industry leaders.

Expert Team:
Our team comprises experienced data managers, biostatisticians, and clinical research professionals who are dedicated to delivering high-quality results.
Regulatory Expertise:
We stay updated with evolving regulatory requirements and guidelines to ensure your data complies with international standards.
Customized Solutions:
Our team handles the collection, assessment, and reporting of individual case safety reports, ensuring adverse events are properly documented and reported to authorities.
Efficiency and Accuracy:
Our commitment to data accuracy, efficiency, and timely delivery sets us apart. We make sure that your data is clean, accurate, and readily available for decision-making.
Cost-Effective Solutions:
Orcitrials offers competitive pricing to suit a range of budgets without compromising on quality.Choose Orcitrials for Clinical Data Management, and experience a seamless, precise, and compliant data management process that accelerates your clinical trials and research projects.

At OrciTrials, we excel in precision and innovation, offering global clinical research solutions tailored to your needs. With decades of experience and a commitment to excellence, trust us to elevate your projects and advance medical breakthroughs for a healthier world.

Pakistan Office 🇵🇰

Level 5, 10-A, Phase 6C
DHA, Lahore, Pakistan

UK Office 🇬🇧

Regus, Office 206, Central Boulevard, Blythe Valley Business Park, Solihull, England, B90 8AG

Singapore Office 🇸🇬

20 Collyer Quay, #09-01, Singapore 049319

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