Accelerating your drug development and approval
Drug development & approval

About us

Pharmavize has been in the business for over 20 years, providing the highest possible standard of CMC development services to a broad customer base from starting companies to tier-one pharmaceutical companies.

Our clients know us as problem solvers who can create made-to-measure solutions to fit their individual requirements.

Pharmavize operates an audited 1,600-m2 GMP facility serving clients from all over the world, including Europe, the United States and Japan. We are thoroughly familiar with the European and American regulatory frameworks and guarantee compliance with all applicable guidelines and directives.

What makes us different?

  • We focus on the development and manufacture of early phase clinical supplies and small-scale commercial batches
  • We have dedicated project teams with unparalleled expertise and responsiveness
  • We provide you with consistent technical reports and compliant regulatory dossiers