As specialist within GCP, GLP and GMP, Tina has more than 25 years of experience with project management, CMC and QA within pharmaceutical development.  She has worked with CRO’s and startup pharmaceutical and medical device companies.

Tina has managed pharmaceutical development projects, built several Quality Management Systems, and audited numerous CRO’s, CMO’s, laboratories and clinics.  She has had several operational and senior management roles within Quality Management, with strong focus on preclinical and clinical research, both in large global corporations’ headquarters as well as in local public entities small startup companies and public organizations. Tina combines a strong focus on end-user needs with solid GxP knowledge and sound business understanding.

Based on her long experience and exposure to best-practices, Tina quickly identifies opportunities for simplification, builds strong commitment and has a hands-on approach to solving issues.  As auditor, she recognizes the strengths of audits as tools to improve and further develop collaborations and processes.