Sylvia is a highly accomplished pharmaceutical professional with more than 15 years of experience spanning early‑stage clinical development through to full commercial readiness. She has a proven track record of supporting cross‑functional teams, optimizing operational processes, and contributing to the successful advancement of therapies across the development lifecycle.
Specializing in Good Clinical Practice (GCP), Sylvia supports pharmaceutical and biotech organizations in achieving robust clinical and laboratory compliance. Her expertise includes GC(L)P consulting, conducting audits, overseeing qualifications, and leading the implementation of Quality Management Systems (QMS).