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Smart Programming and Analysis Computing Environment (SPACE)

Collaborate More Effectively and Efficiently

A single biostatistics and programming solution for clinical study design, management, and regulatory review, Saama’s Smart Programming and Analysis Computing Environment (SPACE) is designed to remove much of the frustration felt by clinical data programmers and biostatisticians.

This efficient, collaborative work environment makes it much easier for users to:

  • Access and ingest current and historical data from a Clinical Data Repository
  • Write, review, edit, and run programs in any IDE (SAS, Jupyter, Visual Studio, Rstudio, NONMEM, etc.) while maintaining strict version control
  • Leverage industry best practice version control with git in the SPACE application
  • Conduct self-service exploratory analytics (descriptive and machine learning-based predictive)
  • Generate valid submission datasets in STDM, ADaM, and TLG formats

SPACE Helps Programmers & Biostatisticians Accelerate Their Work

PACE

A Statistical Computing Environment Designed Just for Pharma

SPACE’s modern design and built-in flexibility eliminates complexity when it comes to critical activities, such as providing access to quality data, TLF generation, and CDISC dataset formatting. When integrated with Saama’s Clinical Data Hub, SPACE delivers a powerful, end-to-end solution for the critical data submission pathway.

To learn more about SPACE and arrange a demo, contact us!

Terms & Conditions

By inquiring about Saama’s Database Lock in a Day, you agree to be contacted by Saama and to allow Saama to use, maintain, store, and protect your personal data in accordance with our Privacy Policy.

Eligibility details are for informational purposes only. Saama, in its sole discretion, will determine your eligibility based on the information you disclose as part of the intake process. If Saama determines that you are eligible to participate, you will be notified by separate email. Eligibility depends on certain criteria, such as the size of your company, the types of clinical trials you sponsor, and the number of patients in–and stages of–your current clinical trials.

By completing the request form, you represent that you have authority to proceed on behalf of your company. Should you agree to participate, you agree to reasonably cooperate with Saama in following the guidelines and procedures required for integrating, standardizing, and analyzing your data. Participation requires the use of our Smart Data Quality application, a technology-agnostic AI engine that sits on top of your current infrastructure. The application can be used immediately, and you’re only charged for the services you use based on a predetermined estimate.

Information you share with Saama during your participation may be anonymized and/or aggregated, and made available publicly in Saama marketing materials. This information may include: types of systems and processes involved, types of departments involved, and size and regional location of your company. Such information will never be directly associated with you, nor will you or your company be identifiable without express written permission.