Clinical Trial SAS Programming

At Pharmnova, we offer robust SAS programming services to support clinical trials by turning complex datasets into actionable insights. Our team of experienced SAS programmers ensures efficient, accurate, and compliant data analysis, enabling sponsors to make informed decisions and meet regulatory requirements with confidence.

Our SAS Programming Services Include:

SDTM and ADaM Dataset Creation

Development of standardized clinical trial datasets based on CDISC standards, ensuring data consistency and regulatory compliance.

Statistical Analysis Programming

Generating statistical outputs, including tables, listings, and figures (TLFs), to support clinical study reports (CSRs) and regulatory submissions.

Data Cleaning and Validation

Ensuring the accuracy, consistency, and quality of clinical data through rigorous data cleaning and validation processes.

Integrated Data Analysis

Combining datasets from multiple studies for integrated summaries of safety (ISS) and efficacy (ISE) to support regulatory submissions.

Custom Programming Solutions

Tailored SAS programming for unique project requirements, including exploratory data analysis and ad hoc reporting.

Automated Processes

Developing automated SAS macros and programs to streamline repetitive tasks, saving time and improving efficiency.

Support for Interim Analyses

Providing real-time programming support for interim analyses, ensuring timely decision-making during clinical trials.

Data Management & Analysis

Efficient data processing, validation, and integration for clinical trials.

End-to-End Documentation

Comprehensive documentation of programming processes, datasets, and outputs to ensure audit readiness and traceability.

Compliance with Regulatory Guidelines

Adherence to global regulatory requirements, including FDA, EMA, and ICH-GCP guidelines, ensuring the readiness of deliverables for submissions.

Why Choose Pharmnova for SAS Programming?

Experienced Team

Highly skilled SAS programmers with expertise in clinical research and regulatory compliance.

Expertise

Familiarity with global standards, including CDISC, SDTM, ADaM, and TLFs.

Customized Solution

Efficient and scalable solutions tailored to meet your study needs and timelines.

Quality and Compliance

Commitment to delivering high-quality, error-free, and compliant deliverables.

 

Transforming Clinical Data into Meaningful Insights!

With Pharmnova’s SAS programming services, you can trust us to provide accurate, timely, and insightful data analysis that supports the success of your clinical trials.

Partner with Pharmnova to harness the power of SAS programming for your clinical research.