At CS Clinical, our team boasts 19 years of experience in clinical data analysis, covering over 350 studies across all development phases, from Phase 1 to Phase 4 and extending to post-approval publication support.
Our portfolio spans a wide array of therapeutic areas, including CNS, infectious diseases, cardiovascular, oncology, skin diseases, respiratory conditions, etc. This diverse experience underlines our capability to handle the unique challenges of different medical fields.
We are also proficient in integration projects, notably ISS/ISE for NDA or sNDA submissions, where meticulous data integration and analysis are paramount.
We rigorously adhere to CDISC standards, ensuring the highest quality and compliance in our processes.
As part of the CS Ltd umbrella brand (www.csltd.com.ua), CS Clinical gains financial stability and access to the talent pool of our parent company. This association enhances our capacity to provide top-quality biostatistics and statistical programming services in the dynamic field of clinical research.
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350+studies
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19+years of experience
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CDISCstandards
We offer statistical and programming services at every stage of new drug development
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Biostatistics
Do you need help developing statistical section for a new protocol, or an SAP? Our statisticians can help.
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Statistical Programming
Our experienced consultant programmers can augment your team to boost your productivity.
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01Discuss the customer’s current biometrics situationDiscuss the customer’s current biometrics situationDiscuss the customer’s current biometrics situation
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02Identify where the customer’s team is understaffed or lacks expertiseIdentify where the customer’s team is understaffed or lacks expertiseIdentify where the customer’s team is understaffed or lacks expertise
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03Allocate our consulting team to address the issues, agree the terms of the engagementAllocate our consulting team to address the issues, agree the terms of the engagementAllocate our consulting team to address the issues, agree the terms of the engagement
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Result
With our help the customer’s team is empowered to do more
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Only High-end PracticesWe take multiple steps to ensure the highest quality
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SOP
All procedures are documented in Standard Operation Procedures documentation and are strictly adhered to.
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FSP
When working under the FSP model, our programmers will adopt your team’s process, SOPs and quality standards.
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Specifications
Programming starts with specifications. Specs define analysis dataset structure.
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Double-programming
We always do 100% Quality Control by independent double-programming.
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Status Tracking
We use centralized status tracking, so that we always know which outputs are in progress, ready for validation, passed validation.
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Access to Specialized Expertise and Customized Services
Our clients get direct access to our specialized biostatistics and programming expertise spanning a wide range of therapeutics areas and statistical methods. Our ability to customize services under each FSP contract ensures that we meet the specific needs and objectives of our clients. This personalized approach aligns perfectly with each project’s goals, maintaining high standards of quality and efficiency.
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Flexibility, Scalability, and Cost Efficiency
The FSP model offers flexibility and scalability, enabling partners to adjust resource allocation in line with the dynamic demands of clinical trials. This adaptability is essential for managing the varied phases of clinical research effectively. Additionally, the FSP contract structure allows for predictable budgeting and cost management, making it a financially prudent choice for our partners. This aspect is particularly beneficial in the face of the financial uncertainties often associated with clinical research projects.
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Strategic Collaboration
The FSP model fosters long-term, strategic partnerships, positioning us as an extension of our clients' teams. This collaborative approach builds trust and ensures cohesive progress toward shared research goals.
How to get started