Regulatory Compliance
21 CFR Part 11, GMP, WHO-GMP, data integrity requirements
Industries
Pharmaceutical Automation Solutions
Engineer Smarter, Safer and Fully Compliant Pharmaceutical Manufacturing
From process automation and 21 CFR Part 11 SCADA to AI-powered vision inspection and complete packaging line integration, Vis-Con Automation delivers pharmaceutical automation solutions that improve productivity, ensure regulatory compliance, and maintain consistent product quality across every stage of pharmaceutical manufacturing.
- Sectors
- 9 focus sectors
- Expertise
- Domain-specific control
- Duty
- 24/7 industrial
- Compliance
- 21 CFR · GAMP 5
Sector brief
Pharmaceutical focus
From process automation and 21 CFR Part 11 SCADA to AI-powered vision inspection and complete packaging line integration, Vis-Con Automation delivers pharmaceutical automation solutions that improve productivity, ensure regulatory compliance, and maintain consistent product quality across every stage of pharmaceutical manufacturing.
Pharmaceutical · engineered, validated, supported
Compliance envelope
Every architecture we hand over in this sector is built to satisfy the standards below from day one — not retrofitted to them later.
- 21 CFR Part 11
- GMP
- WHO-GMP
- EU Annex 11
- GAMP 5
- FDA Data Integrity
- ISA-95
- ISA-88
- ISO 9001
Where we apply it
Oral Solid Dosage Manufacturing
Injectable Manufacturing
Tablet & Capsule Packaging
Vision-Based Quality Inspection
Batch Recording & Process Monitoring
Utilities & Plant Monitoring
Production Line Integration
Industry pain points
What slows this sector down
The recurring constraints we are called in to remove — and the reason most of these plants automate in the first place.
Manual Inspection Errors
Packaging defects, incorrect labels, missing components, damaged seals
Limited Production Visibility
No centralized monitoring, analytics, alarms, trends, batch tracking
Batch Traceability
Batch records, audit trails, electronic signatures, production history
Downtime & Equipment Reliability
Machine failures, maintenance issues, production interruptions
Multi-System Integration
PLCs, SCADA, vision, packaging machines, ERP, MES into one environment
Our answer
How Vis-Con solves them
Each pain point maps to an engineered capability you can open and read in full.
Outcomes
Measurable results
Improved product quality
Higher regulatory compliance
Complete batch traceability
Reduced manual inspection errors
Faster production cycles
Lower manufacturing downtime
Improved OEE
Scalable pharmaceutical manufacturing
Technology
Platforms & protocols
- PLC: Siemens · Allen-Bradley · Schneider · Mitsubishi · Omron · Delta
- SCADA: Ignition · WinCC · FactoryTalk · AVEVA · Wonderware
- Vision: AI Vision · Machine Vision · OCR/OCV · Barcode Verification · Thermal Vision
- Comms: OPC UA · Modbus TCP/IP · Profinet · Ethernet/IP · MQTT
ReferencePharmaceutical — frequently asked
Tap to open
What is 21 CFR Part 11 compliance?
FDA regulation governing electronic records and signatures — audit trails, secure data, validated systems for pharma manufacturing.
Why are machine vision systems used in pharma?
High-speed verification of labels, blister packs, printed info and product integrity with complete inspection records.
Can automation improve GMP compliance?
Yes — validated monitoring, electronic batch records, and audit-ready reporting strengthen GMP compliance.
Which PLC and SCADA platforms do you support?
Siemens, Allen-Bradley, Schneider Electric, Mitsubishi, Omron, Delta; Ignition, WinCC, FactoryTalk, AVEVA, Wonderware.
Do you provide turnkey pharma projects?
Yes — engineering, development, integration, commissioning, validation, training, and AMC support.
Explore more
Related industries
Start a conversation
Automating Pharmaceutical?
Talk to a Vis-Con automation engineer about your facility, its constraints and the compliance you need to satisfy.
VIS-CON AUTOMATION — INDUSTRIAL SYSTEM INTEGRATOR
GANDHINAGAR, GUJARAT · PAN-INDIA DELIVERY