Top 5 Data Storage Mistakes Costing Pharma Companies Compliance & Control

The Hidden Crisis in Pharma Data Management

If you’re a QA/QC manager, operations head, or VP in a pharma company, here’s the truth:
You’re sitting on a goldmine of data—one that could either safeguard compliance or expose you to serious regulatory risk.

Temperature logs. Audit trails. Deviation records.
These aren’t just data points—they’re evidence of compliance, product safety, and operational control.

Yet for many pharma teams, critical data is:

• Trapped in isolated systems
• At risk during infrastructure failures
• Difficult to retrieve when auditors come knocking

And that’s exactly how regulatory gaps, delays, and product recalls begin.

What Pharma Teams Are Silently Struggling With

We’ve worked with top pharma professionals—directors, validation engineers, QA teams—and the pain points are consistent:

• Collecting audit-ready data across sites is a nightmare.
• Our logs are spread across USBs, laptops, and SD cards.
• One power outage and we lose critical records.

These aren’t minor glitches—they lead to non-compliance, delays, and losses.

1. Scattered Data across Devices

Problem: Data stored on USBs, laptops, and SD cards is hard to trace or validate.
Fix: Use cloud-connected data loggers to centralize all data storage in one place across multiple sites—ensuring easy access, traceability, and zero manual syncing.

2. Weak Data Integrity Controls

Problem: Inadequate compliance with 21 CFR Part 11, WHO PQS, or ALCOA+ leads to audit failure.
Fix: Choose loggers with digital signatures, audit trails, and role-based access that strengthen both data storage security and regulatory compliance.

3. Lack of Real-Time Monitoring

Problem: Deviations are often caught too late, after damage is done.
Fix: Deploy Wi-Fi or GSM loggers with live dashboards and instant alerts. With cloud-based data storage, you can review events as they happen—and act before a breach escalates.

4. Data Loss during Power Outages

Problem: Power failure = lost logs = audit risk.
Fix: Use devices with on-board memory and auto recovery features to safeguard data storage even during outages, ensuring no logs are lost.

5. Overloaded Local Storage

Problem: Pharma sites generate massive data, and local systems can’t scale.
Fix: Shift to cloud-based data storage that offers fast, searchable access to historical logs—keeping your operations streamlined and always audit-ready.

Want to Fix These Before Your Next Audit?
At G-Tek, we help pharma teams overcome these exact challenges with:
• 21 CFR Part 11-compliant systems
• Cloud-enabled infrastructure
• Real-time monitoring & alerts
• Secure, audit-ready logging
Don’t wait for an inspection to reveal what’s broken.

Contact us today to turn your data into your greatest asset—not your weakest link.