Sterile manufacturing environments are open to many
sources of potential contamination if not managed correctly.
The need to ensure the safe and sterile transfer of active
pharmaceutical ingredients and formulation ingredients
during aseptic processing has driven the development of
multiple techniques that can be employed in cleanroom
environments to minimise the risks from contaminants.
Christian Dunne, Global Product Manager at ChargePoint
Technology, explores approaches to sterile processing and
compares several techniques.