Aneela is a qualified electronics engineer with over 12 years of experience in the medical devices industry, including 4 years of research and development at the University of Auckland Bioengineering Institute, 6 years of manufacturing, service and support at leading medical device manufacturers and 2 years of regulatory experience. Aneela is a Scheme Manager and Technical Expert for the Active Devices team at BSI Healthcare and is experienced in auditing to the Medical Device Directive 93/42/EEC and FDA 510k submissions
In addition she is a BSI trainer for MDD 93/42/EEC, ISO 14971 Risk Management, Post Market Surveillance and Vigilance, Process Validation and Technical File Writing.
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