Segregation of production to satisfy the needs and desires of
our medical and pharmaceutical customers has been a requirement
we have been pleased to achieve and to continue to grow. With
the third clean manufacturing area now expanding rapidly to meet
contract needs we will continue to focus on future improvements.
The development of these areas has helped in
training for GMP
and also been preferred by our customers through the validation
process and the various phases of trials towards production of a
device.
By incorporating our in house developed cleaning process
adjacent to each of these clean manufacturing areas has also
enabled us be more effective in controlling the process flow.
