Free Guide: How Regulated Labs Use ELNs and Digital Workflows to Ensure Compliance
Discover how Biotech and Pharma labs are reducing audit prep time, minimizing risk, and achieving 21 CFR Part 11 and GMP compliance with less manual work.
Why Compliance Automation is Becoming Essential in Regulated Labs
Manual processes, fragmented SOPs, and unstructured data continue to challenge QA and RA teams under growing regulatory pressure. This free guide explains how labs are digitizing compliance. Not just for inspections, but for daily operational control.
This guide walks you through:
- Real-time compliance dashboards for effortless tracking
- GMP and FDA 21 CFR Part 11-ready workflows
- Automated error validation and audit trails
- Secure electronic signatures for documentation
You’ll learn:
- The 3 biggest risks of manual compliance workflows, and how to eliminate them
- What ALCOA+ means in daily lab practice (and how to enforce it digitally)
- How validated e-signatures and audit trails are transforming inspections
Format: PDF, 6 pages. Instant access after form submission.
Download the Compliance Automation Guide for Regulated Labs
Includes practical strategies to improve data integrity, streamline documentation, and stay inspection-ready without adding manual workload.
How Scifeon Helps You Stay in Control of Compliance
Struggling to stay on top of signatures, files, and inspections? You’re not the only one.
For many lab professionals, compliance is a daily balancing act. Chasing down SOP confirmations, reconciling Excel sheets, or prepping for audits with scattered documentation can drain time and focus.
Whether you’re working in QA, regulatory affairs, or managing operations, keeping everything compliant while staying productive is a real challenge. That’s why Scifeon combines the structure of a LIMS with the flexibility of an ELN, so you don’t have to piece together tools that don’t fit.
What Scifeon helps you do
- Track SOPs and training records without chasing emails
- Automatically log changes and approvals in a clean audit trail
- Record results, metadata, and signatures in a validated ELN
- Configure workflows for deviations, logbooks, or quality events — without IT
- Scale your setup over time or launch full functionality from day one
Scifeon isn’t just about digital tools. It’s about giving you space to focus on quality, instead of paperwork.
Want to see how Scifeon could support your role?