Full Name
Rose Campasano
Professional Title
Principal Consultant
Company
Criterion Consulting LLC
Speaker Biography
I’m a transformation and compliance leader who helps pharmaceutical and life-sciences organizations operate confidently in regulated, data-driven environments.
Today I serve as Principal Consultant, Global Compliance & Enterprise Systems at Criterion Consulting, focusing on the intersection of regulation, operations, and technology. This chapter is especially meaningful as I get to partner with my son, Matt Campasano, founder of Criterion.
What makes my background a bit unique is the combination: multi-country regulatory requirements (FDA/DSCSA, EU, LATAM, Middle East), pharma supply-chain execution (L4/L5 traceability, serialization), and hands-on auditing, SOPs, and policy governance. That blend lets me translate laws and standards into clear, auditable processes teams can run—and auditors respect.
Focus areas
NDC12 migration and DSCSA readiness
Global traceability (L4/L5) and serialization programs
Quality, auditing, SOP and policy frameworks; enterprise systems & master data governance
Cross-functional coaching: turning regulatory change into stable, day-to-day operations
Earlier roles span VP Industry Solutions at LSPedia, Global Professional Services leadership at rfxcel/Antares Vision Group, shared-services transformation at Wolters Kluwer, and IT compliance at Astellas. I also founded ARC Pharma Pro to support clients with SOP creation, contract reviews, and DSCSA readiness.
I believe transformation works when technology, quality, and compliance speak the same language. My aim is to turn complexity into well-governed operations that build trust, readiness, and resilience.
Today I serve as Principal Consultant, Global Compliance & Enterprise Systems at Criterion Consulting, focusing on the intersection of regulation, operations, and technology. This chapter is especially meaningful as I get to partner with my son, Matt Campasano, founder of Criterion.
What makes my background a bit unique is the combination: multi-country regulatory requirements (FDA/DSCSA, EU, LATAM, Middle East), pharma supply-chain execution (L4/L5 traceability, serialization), and hands-on auditing, SOPs, and policy governance. That blend lets me translate laws and standards into clear, auditable processes teams can run—and auditors respect.
Focus areas
NDC12 migration and DSCSA readiness
Global traceability (L4/L5) and serialization programs
Quality, auditing, SOP and policy frameworks; enterprise systems & master data governance
Cross-functional coaching: turning regulatory change into stable, day-to-day operations
Earlier roles span VP Industry Solutions at LSPedia, Global Professional Services leadership at rfxcel/Antares Vision Group, shared-services transformation at Wolters Kluwer, and IT compliance at Astellas. I also founded ARC Pharma Pro to support clients with SOP creation, contract reviews, and DSCSA readiness.
I believe transformation works when technology, quality, and compliance speak the same language. My aim is to turn complexity into well-governed operations that build trust, readiness, and resilience.
Speaking At
