Quality assurance of our pharmaceutical equipment is implemented under strict management. Parts are inspected to determine whether they have been produced according to design.
For important parts, records are made of measurement results and, at the same time, material certificates are secured. As equipment is assembled with parts that have passed inspection on receipt, we verify that the equipment will operate according to the URS.
Later, inspections are done at the plant with the user present. We then agree with the client on when to ship and install the equipment.
Design Quality Verification
After equipment has been produced, we verify that the performance and functions are as indicated on the respective specification sheets of the hardware and software that make up the system.
Factory Shipping Test
With the customer present, we verify that the performance and functions are as indicated on the respective specification sheets, and the hardware and software that make up the system are operated under simulated usage conditions.
Site Acceptance Testing
After the system has been delivered to and installed at the customer's site, we verify that the system can reproduce its performance and functions, etc., and offer IQ and OQ technical support.