Manufacturing Software for Pharmaceuticals
FDA 21 CFR Part 211 compliance, digital production records, and complete lot tracking for pharmaceutical manufacturers.
Challenges in Pharmaceutical Manufacturing
FDA Compliance
Meeting 21 CFR Part 211 and cGMP requirements.
Production Records
Complete documentation for every production run.
Validation
System validation and audit readiness.
How Fiddle Solves These Challenges
Digital Production Records
FDA-compliant production records with e-signatures.
Complete Traceability
Full lot tracking from materials to distribution.
Validation Support
IQ/OQ/PQ documentation and audit trails.
Features for Pharmaceuticals
Formula Management
Manage formulations with version control.
Production Control
Schedule and track production orders.
Audit Trails
Complete audit logging for compliance.
Key Features for Pharmaceutical Manufacturing
Explore the Fiddle features that matter most to your industry.
21 CFR Part 211 Production Records
Create GMP-compliant production records with all required documentation.
Component Lot Traceability
Track APIs, excipients, and packaging from receipt through distribution.
Formula & Potency Management
Build drug product formulas with exact potencies and specifications.
Production Planning
Schedule production based on component availability and release status.
Trusted by Pharmaceutical Businesses
See how companies like yours have transformed their operations with Fiddle.
Fiddle has completely transformed how we manage our inventory. We've reduced stockouts by 80% and saved countless hours on manual tracking.
Ready to Transform Your Pharmaceutical Operations?
Join thousands of businesses using Fiddle to streamline inventory and manufacturing.