Quality by simplicity
At Inno4Life we design smart compact reliable production equipment for the pharmaceutical packaging industry to maximise the ergonomic use for operators and to increase cleanroom efficiency.
With the unique Inno4Life Design Verification methodology and documentation set, up to 80% of the on site validation time required to start production can be saved
All products and services satisfy the stringent requirements of highly regulated markets and comply to regulatory and industry standards and guidelines such as;
- Current Good Documentation Practice (cGDP)
- Good Automated Manufacturing Practice(GAMP 5)
- Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment (ASTM E 2500-7)
- Food and Drug Administration (FDA) predicate rules
- Pharmaceuticals and Medical Devices Agency (PMDA) predicate rules
- European Medicines Agency (EMA) MA
- ICH guidelines
Feel free to contact Inno4Life for any questions on our quality standards.