Mike Halliday has extensive pharmaceutical manufacturing management and QA experience, gained over 20 years working for three major international pharmaceutical manufacturers. Before joining NSF in 2003, he was Associate Director, Global Audit and Compliance for Wyeth Europa. He was also previously a partner at David Begg Associates (DBA).
Mr. Halliday is eligible to act as a Qualified Person and is an honorary lecturer at the University of Strathclyde.
He has broad experience in the manufacturing management and QA of a wide range of sterile and non-sterile dosage forms and is fully conversant with current EU and FDA GMP regulations and requirements. He has extensive experience in international QA auditing of a wide range of pharmaceutical manufacturers and specialist distributors in Europe, the Middle East, America and Asia Pacific.
Areas of recognised expertise include:
- QP training
- Packaging and labelling control
- GMP legislation
- API manufacture and control
- Auditing and self-inspection skills – Education of auditors
- Supply chain distribution