Applying our knowledge and experience GPB provide support to identify and define opportunities for improvement in each process of your medical device life-cycle to maintain compliance and enhance efficiencies.
Our practical Performance Improvement Process collates the necessary data (see Data Analysis) to specify Key Performance Indicators (KPI) to drive improvements or as appropriate maintain:
Product Safety & Performance. (reduce customer complaints / returns)
QMS & Processes Efficiency. (reduce error, costs and time)
Regulatory Compliance. (reduce Notified Body NCR’s & maintain certification)
Evidence of compliance with Harmonised / Consensus / National / International Standards (reduce risk)
Competency of Personnel (enhance contribution through Training)