Validated SAS PC Solution logo

Validated SAS PC Solution

GLP and GCP-compliant SAS PC validation in secure cloud environment for biopharma analysis.

Visit website

Overview

The Validated SAS PC Solution from Circulant Solutions Inc. is a comprehensive SAS PC Validation Package designed specifically for emerging biopharma and therapeutics companies. It enables organizations to conduct statistical analyses within a validated cloud environment that fully complies with GLP (Good Laboratory Practice) and GCP (Good Clinical Practice) standards, helping them bring products to market faster while meeting regulatory requirements.

Circulants Inc. positions itself as more than a technology vendor — the company acts as a committed partner to biopharma and therapeutics clients, helping them navigate the complexities of compliance and infrastructure validation so they can focus on developing innovative therapies.

Key Capabilities

  • Setup of a secure and compliant cloud environment tailored for SAS-based analyses
  • Implementation of proper security policies to protect sensitive data
  • Provision of comprehensive documentation to support all compliance needs
  • Adherence to GLP and GCP regulatory standards throughout the validated environment
  • A solid foundation designed to support future upgrades to SAS Server and additional services

Who It Is For

  • Emerging biopharma companies requiring a validated analytical environment
  • Therapeutics organizations needing to streamline regulatory compliance processes
  • Life sciences teams seeking a scalable, fit-for-purpose SAS infrastructure

Circulant Solutions Inc. is headquartered in Pleasanton, California, and specializes in IT solutions for the bio-pharma sector. Their solution accelerators in clinical and commercial spaces are designed to save clients time and money, with flexibility and scalability to meet evolving market needs.

Meta

Domain
Quality, Compliance & Regulatory
Subdomain
Computer System Validation (CSV)
Software type(s)
Workflow Automation
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
PharmaBiotech
Development stage(s)
Preclinical / Pre-MarketClinical
Target user(s)
Bioinformatician / Computational ScientistQA / Regulatory AffairsIT / Systems Admin / Data Engineer
Compliance standard(s)
21 CFR Part 11GxPISO 27001