T
TARA
TAVARA ERP Assistant
End-to-end pharma operations with drug registry, formulation management, stability testing, FDA/EMA/PMDA regulatory submissions, clinical trial tracking, and complete audit trails for GMP compliance.
Common pain points that TAVARA ERP eliminates for pharmaceuticals businesses.
Strict regulatory compliance (FDA, GMP, 21 CFR Part 11)
Batch and lot traceability from raw materials to finished goods
Quality control at every production stage
Temperature-sensitive inventory and expiry management
Complex clinical trial management across multiple sites
Regulatory submissions to multiple global agencies
Join pharmaceuticals businesses running on TAVARA ERP. Start your 14-day free trial.