Pharmaceutical Serialization Platform for Global Compliance
At a Glance
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Built by Software & Pharma Experts. Trusted by Global Manufacturers.
How we build long-term trust in regulated environments
Integrity
We operate in regulated environments where accuracy, auditability, and accountability are part of how work gets done. Every decision we take is aligned with compliance, data integrity, and long-term trust.
Client Focus
We adapt our solutions to real operational pharma realities across production lines and sites, IT ecosystems, and regulatory pressures. Our role is to reduce complexity, not add another system to manage.
Operational Reliability
Our software and hardware are designed to perform consistently under regulatory, technical, and operational pressure.
Proven Expertise
With 22+ years in pharmaceutical serialization and track & trace, we combine regulatory knowledge, engineering, and software development into one ecosystem.
Because in regulated pharma environments
Global Standards. Enterprise Technology. Proven Compliance.
GS1-aligned solutions, powered by Microsoft Azure, designed for pharmaceutical operations.
Client Experiences That Speak Volume
“SoftGroup delivered a user-friendly, technology-driven platform built on collaboration and trust. As a small company, having partner that understands our needs and provides the right tools is invaluable. SoftGroup’s experitse makes them a truly reliable serialization partner.”
“The flexibility of SoftGroup’s solution and its ability to connect to multiple systems is a real advantage for a small MAH like us. What makes SoftGroup stand out is their personal, hands-on support. We’ve felt like a priority from the beginning.”
“SoftGroup made our EU HUB onboarding clear, simple, and fully compliant. We had confidence in their team from day one. The knew the EMVS requirements inside out. Their continued support gives us peace of mind in our day-to-day serialization activities.”
Find the Latest News & Insights from SoftGroup
Choosing or Switching a Serialization Vendor? Start Here.
Find answers to the questions pharma teams ask when evaluating, scaling, or replacing their serialization systems.
Not sure where you stand today?
Can we switch serialization vendors without stopping production?
Yes. With a phased approach, production lines continue running while the new system is tested and deployed in parallel. The transition is controlled line by line, without disrupting ongoing operations.
Will we lose data during a vendor switch?
No. Existing product data, serial number pools, and transaction history can be analyzed, mapped, and transferred securely. Data integrity and traceability remain fully preserved.
Do we need to replace all systems when switching vendors?
Not necessarily. Many projects reuse existing hardware, integrations, and processes. The goal is to minimize disruption while improving performance and scalability.
How do we know if our current serialization system is no longer sufficient?
- delays during batch setup or reconciliation
- increasing manual interventions
- difficulties adding new markets or partners
- limited visibility across systems
Why do companies switch serialization vendors?
- lack of scalability when expanding to new markets
- performance issues on production lines
- insufficient support
- cost models that become difficult to sustain over time
What should we evaluate when choosing a serialization vendor?
- scalability across markets and sites
- integration with ERP, WMS, and partners
- regulatory coverage and reporting capabilities
- data integrity and audit readiness
- long-term support and cost structure