1. Digitization & Data Integrity ensuring Compliance

EMMA’s fully digital workflow ensures secure, traceable data capture with minimal validation effort, streamlining regulatory audits and reducing compliance burdens.

2. Benchtop, Modular, and Scalable Design

EMMA’s compact, modular architecture fits seamlessly into any lab environment. Whether scaling across multiple sites or starting with a single deployment, EMMA enables easy standardization and ensures consistent QC practices worldwide.

3. Cost-Efficient Endpoint Reading

Focusing on positive/negative results rather than enumeration, EMMA delivers rapid endpoint determinations, cutting operational costs while maintaining the accuracy required for critical QC workflows.

4. Industry-First Petri dish imaging with the Lid On

Powered by patent-pending optics, EMMA is the only system capable of capturing all data without removing Petri dish lids. This ensures sterility throughout the process and eliminates contamination risks, enhancing reliability and reproducibility.

5. SWAP Model for Maximum Uptime

To minimize downtime, EMMA features a SWAP  model. Entire units can be easily swapped out thanks to a proprietary calibration routine that eliminates the need for re-validation. This ensures the highest uptime guarantee in the market and seamless lab operations.

6. Full Compliance with 21 CFR Part 11 and EU Annex 11

EMMA’s design ensures adherence to global electronic records and electronic signatures regulations, including FDA’s 21 CFR Part 11 and EU Annex 11. This compliance guarantees that your digital data management meets international standards for security, integrity, and traceability, facilitating seamless regulatory audits and inspections.

7. Positive/Negative Focus to reduce validation burden

By prioritizing positive/negative results, EMMA makes validation easy. This focus reduces complexity in data interpretation and expedites validation work, giving your organization a time-to-market advantage.