Professional Clinical Trial Data Management & Statistical Analysis Services

Providing high-quality clinical data management, biostatistics, and statistical programming services for pharmaceutical and biotechnology companies to accelerate drug development success

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Data Management

Comprehensive clinical trial data management solutions including CRF design, database construction, data cleaning and locking

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Biostatistics

Professional statistical consulting, SAP development, statistical analysis reports compliant with regulatory requirements

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Statistical Programming

SDTM/ADaM dataset creation, TFL programming, CDISC-compliant data submission package preparation

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Service Process

Professional Service Process Ensures Project Success

We follow international standards and mature methodologies to ensure high-quality delivery of every project

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Requirements Analysis & Solution Design

Deep understanding of client needs, development of detailed project plans and technical solutions to ensure clear and executable project objectives

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    Project requirements research and assessment

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    Technical solution and timeline development

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Analysis
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Execution
02

Project Execution & Quality Control

Strict execution according to plans, establishment of comprehensive quality management systems to ensure data quality and project progress

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    Standard Operating Procedures (SOP)

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    Multi-level quality review mechanisms

03

Delivery & Continuous Support

On-time delivery of high-quality results with comprehensive follow-up support services to ensure client satisfaction

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    Complete delivery documentation and reports

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    Long-term technical support and maintenance

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Delivery
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Core Advantages

Why Choose LinShutong

We have extensive industry experience and a professional team, providing clients with excellent service experience

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Professional Team

Senior data managers, biostatisticians, and statistical programmers with years of industry experience

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International Standards

Strict adherence to CDISC, ICH-GCP and other international standards to ensure data compliance and submittability

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Data Security

Comprehensive data security management system ensuring confidentiality, integrity, and availability of client data

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Efficient Delivery

Mature project management processes and automation tools ensuring on-time, high-quality delivery

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Customized Services

Flexible customized service solutions based on specific client needs

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Full Support

Comprehensive technical support and consulting services from project initiation to final delivery

Let Professional Data Services Accelerate Your Drug Development

We are committed to providing high-quality clinical trial data solutions for our clients,
helping you accelerate the drug approval process

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Performance Data

Let the Numbers Speak

100+

Successful Projects

50+

Partner Clients

98%

Client Satisfaction

Client Testimonials

What Our Clients Say

The LinShutong team is highly professional and has been very helpful in data management and statistical analysis. Their work quality is high, delivery is timely, and they are a trusted partner.

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Manager Zhang, Clinical Operations Lead at a Pharmaceutical Company

The statistical programming project with LinShutong went very smoothly. They have deep understanding of CDISC standards and the submission package passed regulatory review on the first attempt.

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Dr. Li, Statistics Lead at a Biotechnology Company

LinShutong's data management team works very efficiently. The database design is reasonable, data cleaning is timely and accurate, greatly accelerating our project progress.

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Director Wang, Project Management Lead at a CRO Company

Highly recommend LinShutong's biostatistics services. Their statistical analysis reports are professional and detailed, with accurate interpretation of research results.

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Director Chen, Clinical Research Center at a Top-tier Hospital

FAQ

We Answer Your Questions

We provide data services covering all phases of clinical trials, including Phase I-IV clinical trials, BE studies, and medical device clinical trials for data management, biostatistics, and statistical programming.

Yes, our team is proficient in CDISC standards, including SDTM, ADaM, and Define.xml, ensuring that data submission packages meet FDA, NMPA, and other regulatory agency requirements.

Project duration depends on project scale and complexity. We will communicate with you in detail before project initiation to develop a reasonable timeline and strictly follow the plan.

We have established a comprehensive data security management system, including data encryption, access control, audit trails, and confidentiality agreements to ensure the confidentiality, integrity, and availability of client data.

Ready to Start Your Project?

Let our professional team provide the best solution
for your clinical trial data needs

Free Consultation