IntelliSyncsINTELLISYNCS
PHARMACEUTICALS

GMP-compliant automation
for life sciences

Pharmaceutical distribution demands uncompromising precision. Our validated systems enforce GMP protocols, maintain cold chain integrity, and deliver end-to-end serialization — so every dose is traceable from dock to patient.

Pharmaceutical cold chain warehouse automation
CAPABILITIES

Built for regulatory excellence

Every capability is designed to maintain compliance while driving operational efficiency.

GMP & GDP Compliance
Validated workflows that meet current Good Manufacturing Practice and Good Distribution Practice standards — every process documented, every deviation tracked.
Cold Chain Integrity
Continuous temperature monitoring across all storage and transport zones with automated alerts and corrective-action triggers.
Serialization & Track-and-Trace
End-to-end serialization from manufacturing through distribution — full DSCSA compliance with unit-level traceability.
Audit-Ready Documentation
Automated batch record generation, deviation logging, and audit trail maintenance — pass any FDA or EMA inspection with confidence.
Temperature-Controlled Picking
Zone-based picking in validated 2–8°C and 15–25°C environments, with automated expiry-date prioritization.
Last-Mile Cold Chain
Integration with validated cold chain carriers ensures temperature integrity from your dock to the pharmacy or hospital door.
OUR PROCESS

From validation to scale

A proven methodology for deploying automation in regulated environments.

01

Validate

Map your current GMP workflows and identify automation points that maintain — or enhance — compliance posture.

02

Integrate

Deploy validated automation systems with full IQ/OQ/PQ documentation, integrated to your existing QMS.

03

Monitor

Continuous environment monitoring with automated deviation handling — no manual log checks required.

04

Scale

Add capacity, new temperature zones, or additional product lines without re-validation overhead.

TECHNOLOGY

Regulatory-ready tech stack

We integrate with the systems your quality and regulatory teams already trust.

Regulatory
  • FDA 21 CFR Part 11
  • EU GMP Annex 11
  • DSCSA
Monitoring
  • Sensitech
  • Elpro
  • Vaisala
  • Testo
Integration
  • SAP ATTP
  • TraceLink
  • rfxcel
  • Optel
100%
Audit pass rate
3×
Faster batch release
0
Temperature excursions

Ready to automate your pharmaceutical distribution?

Let’s discuss how our validated systems can accelerate your batch release, eliminate temperature excursions, and keep you audit-ready every day.