Big Benefits, Scalable Price: The SAS® Cloud-Based Clinical Platform for SMBs
Learn how small-to-midsize pharmas, biotechs, medical device manufacturers and CROs can benefit from a compliant cloud-based solution to facilitate clinical trials.
About the webinar
Collecting, managing, standardizing and analyzing clinical trial data is crucial in the clinical submission process for regulatory approval for new medical or biotech devices.
SAS has a scalable solution to help small-to-midsize organizations with the clinical trial process.
We’ll demo the SAS Life Science Analytics Framework and show how it can benefit small-to-midsize organizations (pharma, biotech, medical device and CRO).
What you'll learn:
- How the SAS framework can help define and manage policies to ensure FDA compliance.
- How to easily drive collaboration and workflow between preclinical, biostatistics, operations and medical affairs.
- How you can end the struggle with the management and implementation of clinical data standards (CDASH, SDTM, SEND, ADaM and Define-XML).
- How you can quickly answer regulatory inquiries and trace data pedigree back to the source.