About Mark Vlasic
Mark Vlasic brings over two decades of experience across pharmaceutical manufacturing, technical operations, validation, and project management. His hands-on experience provides a strong foundation in GMP compliance, quality systems, and regulatory frameworks.
He offers a comprehensive and practical understanding of successfully advancing drug and nutraceutical programmes from development through to commercialisation.
In his current role, Mark partners with global clients, leveraging his technical expertise and industry insight to drive strategic growth and enable successful, long-term collaborations.
He offers a comprehensive and practical understanding of successfully advancing drug and nutraceutical programmes from development through to commercialisation.
In his current role, Mark partners with global clients, leveraging his technical expertise and industry insight to drive strategic growth and enable successful, long-term collaborations.
Areas of expertise
Insights by Mark Vlasic
Meet the Douglas CDMO team at AusBiotech 2025
Read articleMeet us at Pharmaceutical Development Conference Sydney 2025
Read articleDouglas CDMO will be at DCAT 2026
Read articleCRO vs CMO vs CDMO: What’s the difference? A guide for pharmaceutical and biotechnology companies
Read articleWork with Mark Vlasic’s team
Talk to Douglas CDMO about formulation, development and manufacturing for your molecule.
Get In Touch