Pharmaceutical Manufacturing ERP
Full GMP compliance, Electronic Batch Records, and automated validation. Turn regulatory pressure into a competitive advantage with Sage X3.
Why RFR for Pharma?
From clinical trials to commercial production, pharmaceutical manufacturers need an ERP that speaks the language of validation. Generic systems require costly customisation that breaks with every upgrade.
Validation comes first, then the software. The team understands IQ/OQ/PQ protocols and ensures your Sage X3 environment is essentially "pre-validated" for faster FDA approval. Electronic signatures, secure audit trails, and role-based security come built in.
Qualified in Three Stages
Validation comes first, then the software. Every Sage X3 environment we deliver is qualified against written IQ/OQ/PQ protocols, so access controls and e-signatures are tested, never assumed.
- IQStage 1
Installation Qualification
Verify the system and its environment are installed correctly, documented, and secured before configuration begins.
- OQStage 2
Operational Qualification
Exercise workflows, electronic signatures, and role-based access controls against approved test scripts.
- PQStage 3
Performance Qualification
Prove the validated process runs reliably under real production conditions, batch after batch.
Field note, anonymised
"RFR's understanding of pharmaceutical validation is what set them apart. Our Sage X3 environment passed FDA audit on the first attempt. The electronic batch records and e-signature workflows they configured saved us months of manual documentation."
Pharmaceutical Expertise
Deep domain knowledge across the pharmaceutical value chain.
- Generic Pharmaceuticals
- Biopharmaceuticals
- Medical Devices
- Contract Manufacturing
- Animal Health