Site closures, modified business models, and competitive strategies of pharmaceutical companies often necessitate outsourcing of drug manufacturing as well as the associated transfer of process responsibilities in nearly every phase of a product life-cycle.
We support you with process development, process validation and validation of analytical methods, commercial production, and sales of your products. Our extremely well-trained transfer teams stand by your side with deep specialized knowledge, experience and dedication in each process phase.
Whatever transfer project you would like to tackle – with us it is in the best of hands and will of course be documented in all transfer phases in a GMP-compliant manner. We know that compliance with regulatory requirements is not all that is necessary. Perfect planning and sustainable documentation are the key factors for a successful product transfer.