Meet FDA and cGMP requirements with confidence. Fiddle provides 21 CFR Part 11 compliant electronic records, complete lot traceability, electronic production records, and audit-ready documentation for food, supplement, and cosmetics manufacturers.
Everything you need to meet FDA regulations and cGMP requirements for manufacturing
Meet FDA electronic record requirements with secure authentication, electronic signatures, and tamper-evident audit trails. Every record change is documented with user attribution and timestamps.
Create, review, and approve production records that meet cGMP documentation requirements. Master production record templates ensure consistency across all production runs.
Track every ingredient and product through your entire supply chain. Achieve FDA traceability requirements with forward and backward lot tracking for instant recall readiness.
Document quality inspections, testing results, and specifications throughout production. Ensure every batch meets quality standards before release.
Maintain complete, audit-ready documentation for FDA inspections. Every action is logged with who, what, when, and why for full regulatory transparency.
Reduce compliance burden with automated workflows that enforce cGMP requirements. Built-in validation rules ensure documentation is complete before proceeding.
Reduce compliance risk, streamline audits, and focus on manufacturing great products
Be prepared for FDA inspections at any time with complete documentation, audit trails, and instant access to production records and traceability data.
Automated workflows and built-in validation rules reduce manual compliance tasks by up to 60%, freeing your team to focus on production.
Meet FDA electronic record requirements out of the box with secure authentication, electronic signatures, and tamper-evident audit trails.
Track every ingredient and product through your supply chain. Execute recalls in minutes with instant impact analysis and affected customer identification.
Replace paper records with digital documentation that enforces completeness and accuracy. Catch errors before they become compliance issues.
Accelerate batch review and release with exception-based review workflows. Reduce batch release time from days to hours.
See how food, supplement, and cosmetics manufacturers achieve compliance with Fiddle
"Our FDA auditor was impressed with how quickly we could pull any production record and trace every ingredient back to its source. Fiddle made our last inspection our smoothest ever."
"Before Fiddle, cGMP compliance was a constant struggle with paper records and spreadsheets. Now everything is documented automatically, and we can focus on making great products instead of paperwork."
See how Fiddle's FDA and cGMP compliance software can simplify regulatory requirements and give you confidence during audits. Schedule a personalized demo today.