Statistical and programming services for smart drug development
agent

Contact us

Providing Statistical Programmers and Biostatisticians

office-roomss
CS Clinical - biometrics CRO

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.

  • 350+
    studies
  • 19+
    years of experience
  • CDISC
    standards
bulbi
Services

We offer statistical and programming services at every stage of new drug development

Roadmap
  • 01
    Discuss the customer’s current biometrics situation
    Discuss the customer’s current biometrics situation
    Discuss the customer’s current biometrics situation
  • 02
    Identify where the customer’s team is understaffed or lacks expertise
    Identify where the customer’s team is understaffed or lacks expertise
    Identify where the customer’s team is understaffed or lacks expertise
  • 03
    Allocate our consulting team to address the issues, agree the terms of the engagement
    Allocate our consulting team to address the issues, agree the terms of the engagement
    Allocate our consulting team to address the issues, agree the terms of the engagement
  • Result

    With our help the customer’s team is empowered to do more

Contact us
  • Only High-end Practices
    We take multiple steps to ensure the highest quality
    builing
  • ss
    SOP

    All procedures are documented in Standard Operation Procedures documentation and are strictly adhered to.

  • FSP

    When working under the FSP model, our programmers will adopt your team’s process, SOPs and quality standards.

  • Specifications

    Programming starts with specifications. Specs define analysis dataset structure.

  • Double-programming

    We always do 100% Quality Control by independent double-programming.

  • Status Tracking

    We use centralized status tracking, so that we always know which outputs are in progress, ready for validation, passed validation.

Our Advantage
  • galka
    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.

  • icon
    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.

  • icon
    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.

    Name

    Email

    Message (optional)

    This site is protected by reCAPTCHA and the Google Privacy Policy  and  Terms of Service apply


    This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply

    Contacts sent
    We will contact you within 24 hours