For more than 20 years Pörner Kundl has been engineering and executing projects for industrial plants  and industrial building services. Project planning encompasses all aspects with all disciplines being available from a single source. In addition to conventional plant engineering our focus is also on:

• Process plants and mechanical building services
• Electrical/Instrumentation and Control
• Validation and Qualification

Pörner Kundl provides all services from one single source necessary for the engineering of pharmaceutical process plants and the associated clean room systems :

• Pre-engineering and feasibility studies
• Independent consulting
• Project management
• Authority approval procedures
• Environmental impact assessments
• Engineering including detail engineering
• Process engineering
• Specification of machines and equipment
• Layout
• Piping plans
• Electrical systems
• Instrumentation and automation
• Tendering and contract award
• Coordination and expediting
• Budget control
• Local construction supervision
• Final documentation

The electrical/I&C components are processed in line with the individual engineering stages, i. e. from basic engineering, specification, coordination of interfaces to other disciplines, tendering and purchasing through to commissioning and final documentation:

• Instrumentation
  • Field instruments (sensors, actuators etc.)
• Automation
  • PLC
  • Control systems
  • Visualization
• Power distribution
  • Transformers
  • Switchgears
  • UPS systems
  • L.V. distribution boards
  • Emergency generating sets
• Cabling
  • Cable trays
  • Bus connections
• Building services
  • Grounding
  • Lightning protection
  • Illumination
  • Data processing and telecommunication
  • Video surveillance systems
  • Fire alarm systems
• Documentation for TÜV acceptance
  • Eex-i system descriptions
  • Explosion protection documents (VETAX)
  • Defining explosion-hazardous zones and concepts

All services connected with the validation and qualification of pharmaceutical process plants, clean rooms, HVAC and computer systems are provided:

• Planning - drawing up of

  • Master plans
  • Risk analyses
  • Validation guidelines and test plans
• Execution
  • DIOQ tests
  • Documentation, tracking and solution of variations
  • Review and release of records
  • Qualification reports
• Management
  • Leading the validation team
  • Planning and control of activities
  • Coordination of interfaces

• Consulting

  • GMP audits
  • Systematic compilation of GMP documentation
  • Preparing SOPs; GMP and Part 11 compliance studies
• Support
  • Preparing company-specific validation systems including guidelines
  • Standards for the qualification of systems (HVAC, media and process)