rantronik supported its customer in particular with its in-depth specialist knowledge and experience in optimizing and supervising processes and rectifying pharmaceutical defects. At the same time, rantronik made a significant contribution to maintaining the necessary motivation during the continuation of production until the transfer was completed.
Last but not least, the task also included the upcoming final qualification of systems and equipment as well as the organization for their continued use at other locations.
On site, rantronik provided advice and support through individual training and assistance to staff in order to transform established actions and behaviors into GMP-compliant actions.
Do you also need support with your transfer processes, the optimization and supervision of production processes, the development of pharmaceutical systems, plant qualifications or process validations and the processing of defect lists?
Contact us at any time - we will be happy to support you and provide you with comprehensive advice on your processes.