Compliance-driven IIoT Connectivity for Pharma Manufacturers
Reduce your risk of FDA warning letters as much as 40%
Reduce your risk of FDA warning letters as much as 40%

Even though most pharma companies know their increased risks, more than half of them still rely on manual data entry and human intervention to fill in the gaps. We all know that technology is necessary to solve this problem, but many solutions can still put you at risk from:
- Incompatibility of software-hardware to connect isolated systems and machines
- Vulnerability to vendor lock dependency
- Lack of proven-record software options
- Unclear return on investment
Address compliance once and for all with the zenon platform
Become FDA Proof
Building a future-proof solution for error-free compliance requires three critical components that are all built-in to zenon software.
Flexibility
Ensure software seamlessly integrates your production floor islands with your current systems (MES, ERP, Process Historian, etc.), no matter the hardware. Is it scalable enough to adapt to your future needs?
Compliance
A modern integration software must always provide full compliance FDA 21 CFR part 11 by using code-free and ready-to-use solutions such as audit trail with eSignature and deviation detection.
Productivity
Error-free compliance is valuable but not at an expense to your productivity.
An ideal solution should boost profitability and add options like ISA-88 batch control.
Ask yourself the value of what each of these mean to your workflow needs and contact COPA-DATA to learn more about addressing compliance once and for all.
Integrate with zenon and avoid the FDA.
Schedule an integration consultation for an FDA-proof and profitability-boosting operation.
Trusted by these companies



