GAMP5 Validated
Pharmaceuticals & Biotech Automation
GAMP5 compliant control architecture, FDA 21 CFR Part 11 compliant audit trails, electronic batch records (EBR), and cleanroom pressure zone cascading.
Pharmaceutical automation is a documentation discipline as much as an engineering one. Every deliverable we produce is traceable to a user requirement and verified through a formal qualification lifecycle.
Sector Capability Matrix
- check_circle Validated electronic signature protocols
- check_circle Critical temperature & humidity interlocks
- check_circle Electronic batch records and audit trails
- check_circle Cleanroom pressure cascade control
Direct Engineering Line
Ready to Optimize Your Plant Operations?
Schedule a technical scoping session with our senior automation engineers in Randburg or request an on-site facility evaluation across Sub-Saharan Africa.