Element’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. Element 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. Element achieves this by adhering to CDISC standards and other important regulatory models such as the SDTM, ADaM, ensuring organizations stay abreast of the latest regulatory requirements.
With Element, you can:
- Standardize and validate clinical trials data
- Refine clinical data with SAS’ advanced analytics to identify risk scenarios and address them before impact
- Seamlessly implement International Standards such as the CDISC by leveraging Element’s cost-effective and flexible engagement models
- Gain access to clinical trials data management expertise and regulatory compliant expertise to enable well-informed clinical development decisions and submissions