Sectors
Pharmaceutical QHSE
GMP compliance and quality excellence
Ensure regulatory compliance and quality of your pharmaceutical products with our comprehensive QHSE management solution.
Pharmaceutical Features
Tools compliant with regulatory requirements
GMP Documentation
Manage your batch records, procedures and specifications.
Quality Reports
Generate product quality reviews and regulatory reports.
Deviation Management
Handle deviations and CAPAs efficiently.
Process Validation
Manage qualification and validation of your processes.
Audit Trail
Full traceability compliant with 21 CFR Part 11 requirements.
Batch Traceability
Track your batches from raw material to finished product.
What Betterfly automates here
GMP document control and deviation handling, with a trace at every step.
GMP and ICH Q10 document control
Procedures, specifications and records in a document system with version control: the current version is always the right one, aligned with GMP, ISO 13485 and ICH Q10.
Tracked deviations and corrective actions
Every deviation is logged, qualified and tracked to closure by the executable BetterFlow engine, with human validation at sensitive points.
Traceability of the copilot's analyses
Every BetterAssist answer carries a trace (cited sources, model, cost); coverage keeps expanding. The copilot augments the expert, it does not replace them.
Pharmaceutical Standards
Compliance with sector regulations
Quality management
Medical devices
Good Manufacturing Practices
Pharmaceutical quality system
Secure your pharmaceutical production
GMP compliance made simple