FleetBioprocessing Deliver

Unrivalled technical expertise in conjugation chemistry, immunoassay development, protein purification and reagent formulation and dispensing, allowing us to fulfil all your development, validation and production needs in these areas.
  • ​Quality standards meeting the requirements of ISO9001, and ISO13485, and consistent with the Quality System Regulations of the US Food and Drug Administration (FDA).
  • Full consultation throughout the progress of a project, from quotation through to delivery 
  • The responsive approach and highly competitive price structure achievable by a small dynamic company. Depending on the work involved, contracts range from a few days to phased immunoassay development projects extending over many months with regular design reviews and feedback meetings.  
Fleet Bioprocessing are certified to ISO9001 : 2015 and ISO13485 : 2016, which emphasise continuous improvement and customer satisfaction as well as demanding robust and effective quality standards.
Fleet Bioprocessing also possess considerable experience in the development and optimisation of processes, including the use of techniques such as Failure Mode and Effect Analysis (FMEA) to identify key variables, and Design of Experimentation (DoE) procedures such as the use of  reduced factorial arrays to optimise your "information to experimental effort" ratio.