Our Pharmaceuticals ERP governs from API synthesis to patient delivery, with robust validation, electronic batch records, and pharmacovigilance tools for a highly regulated, life-critical sector.
Streamline your operations with our cutting-edge electronic batch records (ebr) solutions.
Streamline your operations with our cutting-edge serialization and track-and-trace solutions.
Streamline your operations with our cutting-edge stability chamber management solutions.
Streamline your operations with our cutting-edge gmp compliance workflows solutions.
Streamline your operations with our cutting-edge api and excipient inventory solutions.
Streamline your operations with our cutting-edge clinical trial material control solutions.
Streamline your operations with our cutting-edge regulatory submission support solutions.
Streamline your operations with our cutting-edge adverse event reporting solutions.
Streamline your operations with our cutting-edge supply chain risk assessment solutions.
Streamline your operations with our cutting-edge validation lifecycle management solutions.
Reduce audit findings by 50%
Accelerate approvals by 25%
Ensure 100% serialization
Minimize stock discrepancies by 30%
Faster stability data access
Proactive quality deviations
Global filing efficiency
Enhanced patient safety
Discover how we've helped businesses in your industry achieve remarkable results
Generics
Biopharma
Get answers to the most common questions about our Pharmaceuticals ERP solutions
Electronic signatures, audit trails, and automated workflows per 21 CFR Part 11.
Full DSCSA/EMVS support with GS1 standards and aggregator integrations.
Chamber scheduling, data logging, and ICH guideline reports for shelf-life.
Yes, AE intake, signal detection, and regulatory submissions for safety monitoring.