IBS TECHNOLOGIES


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OUR SERVICES



SAS CLinical SErvices



SAS CLINICAL SERVICES




IBS’s SAS Clinical Services enable organizations to meet and be compliant with the changing regulatory requirements. We offer customized solutions that are aimed at reducing operational costs and achieving increased productivity. IBS implements flexible and scalable engagement models to manage your SAS programming requirements.


Our team of qualified SAS clinical programmers are up to date on all the regulatory standards requirement and generate validated clinical study reports and submission ready deliverables. We adhere to CDISC standards and other important regulatory models such as the SDTM, ADaM, etc. ensuring organizations stay ahead of the latest regulatory requirements.



ORGANIZE



Standardize and validate your clinical trials data to organize and prepare for further analysis.



REFINE



Refine clinical data with SAS' advanced analytics to identify and proactively address risk scenarios.



INTEGRATE



Seamlessly implement international standards, such as CDISC, by leveraging IBS' cost-effective and flexible engagement model.



EXTRAPOLATE



With IBS' clinical trials data management expertise and regulatory compliance expertise, unlock well-informed clinical development decisions.



BIOSTATISTICS, CLINICAL SAS PROGRAMMING
& PROGRAM MANAGEMENT CAPABILITIES



Statistical input to Protocol

Sample size Estimation

Randomization

Development of SAP and Mock TLF shells

Statistical section writing for CSR

Safety & Efficacy Analysis and Reporting

Interim Analysis

PK/PD Analysis

Exploratory Analysis

Meta-Analysis

Analysis Dataset (ADaM/Sponsor defined) creation

QC of analysis and reporting

Integrated Summary Support (ISS/ISE)



CONTACT US



sales@ibs-tech.com | Phone: 609.945.5391