To build a system that completely qualifies a Dry Powder Inhaler (DPI) Product based on its ability and efficacy to aerolize and deliver targeted drugs to a patient's lungs.
Integrating an NI CompactRIO (cRIO) controller with FPGA and real-time determinism to instantaneously detect events based on signal signatures.
The end solution is an Automated Test Equipment (ATE), deployed on the production floor for qualifying parts that were manufactured. This consists of test fixture for measuring the flow v/s pressure characteristics of the DPI.
As the system is built for the pharmaceutical industry, it has to conform to the electronic standards for Medical Equipment, namely the US FDA prescribed 21 CFR Part 11 standard. This Includes the implementation of controls such as access controls, audit trials and auditing functions, system validation, electronic signatures, data retention and permanence, and reasonable tamper proofing.