As regulatory expectations increase and supply chains demand faster decisions, laboratories need a smarter approach to sterility testing.
Celsis® delivers:
- Sterility results in as little as 6 days
- Objective analysis with trusted accuracy
- Digital documentation that strengthens data integrity
- Comprehensive support from feasibility through validation
Designed to work in tandem with compendial methods, Celsis enables laboratories to modernize confidently. Validation support packages streamline implementation through method suitability testing, equivalency studies, limit of detection evaluation, and comprehensive documentation.
Thousands of regulator-approved batches have been released using Celsis, helping organizations accelerate time-to-market while maintaining product safety and compliance.
As Pharma 4.0 reshapes manufacturing and quality operations, rapid microbial detection helps align QC laboratories with digital transformation initiatives and supply chain efficiency goals.
Modern sterility testing is no longer just about speed. It is about operational agility, data integrity, and regulatory confidence.
Start your journey toward a faster, more reliable solution.
