For the STEQ America Services team, the customer relationship does not end at the delivery of the equipment. STEQ America Services cares to offer a unique and differentiated after-sales service, focused on customer needs related to the entire state of quality of the process and finished product.
The failure of equipment or misuse can have devastating effects on research results and production. These issues can be magnified by the turnover of staff, lack of knowledge of the equipment or process, and limitations to in-house service or maintenance.
STEQ America understands that facilities often encounter these issues, decreasing the efficiency of the equipment and processes. To assist in the resolution of these issues, and to keep your equipment and processes running smoothly, we have enhanced our customized training and services offerings for our partner lines of equipment.
Execution of IQ and OQ protocols
Technical support / Validation support
Calibration tool supply (vendor specific) and calibration
service for tools
Calibration repair and service for equipment
End user training for system understanding/use
Service, troubleshooting, and calibration training
USP method discussion, application analysis, SOP draft creation (STEQ America supplied equipment only)
Our manufacturing partner, Matachana Group, has been producing premium, small to bulk steam sterilizers for more than 50 years. They provide services in over 110 countries. These sterilizers are engineered for flexibility, and to support your cGMP, QC testing and QC application needs. Have you read their latest publication?
We’ve had some exciting times at STEQ America, recently partnering with even more multinational, pioneering equipment manufacturers to bring you advanced solutions for R&D and manufacturing in pharmaceuticals, biotechnology, and life sciences. Click here to download our new product line flyers and stay current with the innovative technologies you need to be leaders in your industry.
Pharmaceutical production is moving in a new era, one in which personalized medicine and drug-device configurations will be significant areas of interest. This will require equipment to process dedicated and smaller batches, still comply with cGMP, be custom-designed, all while meeting the needs your current operational requirements.