SAS Programming Services

SAS Programming Services

Transform Your Clinical Data into Regulatory-Ready Deliverables

GCP ClinPlus delivers expert SAS programming services to help sponsors convert complex clinical data into submission-ready datasets, tables, listings, and figures. With 22 years of experience supporting over 2,200 successful projects, our specialized team provides the technical expertise and efficient workflows necessary to accelerate your clinical development timelines.

Why Outsource SAS Programming?

SAS programming represents one of the most resource-intensive components of clinical development, often requiring significant scaling during key study periods:

● Variable resource demands throughout development lifecycle

● Specialized technical expertise requiring extensive training

● High overhead costs for maintaining permanent staff

● Productivity fluctuations during submission preparation

Our flexible SAS programming services provide the perfect solution, allowing you to:

● Scale resources efficiently during peak periods

● Reduce overhead costs by eliminating permanent headcount

● Access specialized expertise without lengthy recruitment

● Maintain consistency in deliverables and standards

Our Comprehensive SAS Programming Services

CDISC-Compliant Dataset Creation

● SDTM datasets conforming to the latest implementation guides

● ADaM datasets optimized for statistical analysis

● Define.xml documentation with comprehensive metadata

● Traceability from source data to analysis results

Tables, Listings, and Figures (TLFs)

● Standard safety and efficacy TLFs following industry best practices

● Custom visualizations to highlight key findings

● Submission-ready formats meeting regulatory requirements

● Consistent styling across study deliverables

Statistical Analysis Implementation

● Complex statistical model implementation in collaboration with biostatisticians

● Validated macros for efficient analysis execution

● Reproducible workflows ensuring analysis integrity

● QC processes that minimize errors and ensure accuracy

Submission Support

● Integrated summaries of safety and efficacy (ISS/ISE)

● Legacy data conversion to current standards

● Regulatory submission packages with all required documentation

● Response to regulatory queries with rapid turnaround

The GCP ClinPlus Advantage

Efficient Onboarding

Our proprietary onboarding process ensures new SAS programmers integrate seamlessly with your team:

● Comprehensive knowledge transfer tailored to your specific needs

● Documentation review to understand standards and workflows

● Mentoring program pairing new team members with experienced leads

● Progressive responsibility as team members gain familiarity

Quality Assurance

Our multi-layered quality control process delivers reliable, error-free deliverables:

● Automated validation checks to identify issues early

● Independent code review by senior programmers

● Cross-functional quality control involving statistical oversight

● Continuous improvement through lessons learned

Standards Expertise

We maintain expertise across all relevant industry standards:

● CDISC SDTM and ADaM implementation guides

● Therapeutic area standards for specialized domains

● Sponsor-specific standards for customized implementations

● Regulatory guidance from global authorities

Flexible Staffing Models

Our SAS programming services offer multiple engagement options:

● Full-service outsourcing for complete programming departments

● Functional Service Provider (FSP) for team extensions

● Project-based support for specific study deliverables

● Hybrid approaches combining internal and external resources

Case Study: Efficient Resource Scaling

A US subsidiary of a global ophthalmic pharmaceutical company utilized GCP ClinPlus' SAS programmer FSP services to manage workload fluctuations during peak trial periods. This approach allowed them to efficiently scale their biometrics team without permanent headcount costs—expanding capacity during critical submission preparation phases and reducing it during quieter periods. The model provided immediate access to specialized programming expertise while maintaining consistency in deliverables and regulatory compliance.

Technology and Infrastructure

GCP ClinPlus invests in the infrastructure needed to support efficient SAS programming:

● Latest SAS versions and modules for optimal performance

● Secure collaboration platforms for seamless information sharing

● Version control systems ensuring code integrity

● Validated environments meeting regulatory requirements

Commendation Letter

I want to sincerely thank your team for supporting us with SAS programming at a crucial time. When we faced a sudden need to increase our programming capability, your team quickly made an significant impact. I particularly appreciated your technical skills and smooth collaboration. The datasets and TLFs you delivered were consistently high-quality—accurate, well-documented, and easily integrated into our workflows. It's rare to find a partner who combines high technical skill with great collaboration, and we're very lucky to have found this in you. Thank you again for helping us at such a crucial time. 


Ready to Optimize Your SAS Programming Resources?

Contact us today for a complimentary assessment of your SAS programming needs and discover how our flexible resourcing models can help you accelerate delivery while reducing costs.

Contact: Suling Zhang, VP of International Operations and Business Development
 
Email: suling.zhang@gcp-clinplus.com
 
Phone: 609-255-3581


Recommendations

Global Biometrics Excellence: Powering Clinical Trial Success
Founded in 2003, we are an international biometrics service provider with strategic offices acrossth...
Build or Buy? A Guide to Biometrics Resourcing
The Strategic Crossroads Every Biotech and Pharma Company FacesIn today's increasingly complex marke...
Interpreting the roles and responsibilities of relevant personnel from the perspective of clinical trial data flow
Clinical trial data can be defined as any information or fact related to a clinical trial. What info...
Top 5 Biometrics Mistakes That Delay Clinical Trials
In today's complex clinical development landscape, where trial costs continue to rise and timelines ...