When it comes to handling health-related products such infusion bags, bottles, cartridges or vials before and after sterilisation, special care is required.
ETT’s machines can be designed according to GMP-guidelines if required. They ensure gentle product handling and offer high quality and durability. We also provide support during the equipment qualification and validation processes and compile the associated qualification documents (FDS, HDS, SDS, IQ-/OQ-reports, etc.) if required. Specially trained for pharmaceutical projects, our team can relieve you from this task and ensure smooth and trouble-free implementation of your project. In addition, ETT are able to generate production-relevant data and transmit them to a superordinate control system for compilation of a batch report. And if you do not have a superordinate control system, ETT can compile the batch report directly. When it comes to product tracking, ETT cooperate with Track&Trace experts to meet the requirements for serialisation in the pharmaceutical industry.
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ETT are looking forward to implement your project in close cooperation with you. Send us a non-binding inquiry, our team would be pleased to give you advice.