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With a diverse career spanning five continents, Mike has nearly 45 years of experience in business leadership and diverse technical management in the pharmaceutical industry. At QuVa, Mike’s current roll is focused on increasing all employees’ awareness and adherence to cGMP requirements across all aspects of the business. Previously he led QuVa’s integration of automated solutions while optimizing compounding processes in support of sterile manufacturing and supply chain platforms. Mike and his team continually focus on knowledge transfer and process design to optimize, automate, and advance QuVa’s performance levels and output. His in-depth knowledge of Good Manufacturing Practices and regulatory requirements ensures sustainable, compliant solutions to prevent drug shortages. The establishment of a GMP Compliance Office is yet another sign of QuVa’s growth, maturity, and recognition of what it takes to be the top service provider in the 503B Industry.