Phone: +61 3 9761 8588 Fax: +61 3 9761 8577 Email: firstname.lastname@example.org
Address: Factory 39/65-
The underlying principle driving our applications is the desire to exceed our clients’ expectations on each and every project.
“Just enough is just not good enough.”
Reduced Human Inconsistence
Reliable Delivery of Product
Increased Quality of Goods
Excellent Return on Investment
Ramdraft’s skills in automation are to provide a single source capability from project concept, through project scope, user requirement documentation support, functional description document support, hardware and software design specifications, electrical/instrumentation/automation CAD drawings, PLC programming, HMI/SCADA programming, data historian storage/retrieval, management and production reporting systems, site construction supervision, control system testing and commissioning, operations and maintenance manual technical writing, control system installation qualification, operational qualification and performance qualification support, and control system life cycle maintenance support. Our software and deliverables are designed in accordance with GAMP5 (ISPE – Good Automated Manufacturing Practice Version 5) which is internationally adopted for pharmaceutical automation works to meet FDA (USA), TGA (Australia and New Zealand) and PIC/S (Europe) requirements.
Ramdraft commission and validate plants to FDA standard. They provide systems that capture and monitor data as the factory is running, whether that be materials input, production plant , HVAC systems, water and waste and environmental monitoring. Data collected is used for ongoing monitoring and audit tracking to international standards. Ramdraft provide full documentation including Site Acceptance Tests (SAT), Operations and Maintenance (O&M), Safety Data Sheets, Electrical drawings and Testing, Calibration data and full user manuals. Ramdraft provide full training to staff and ongoing monitoring and support as required.