Senior Regulatory Affairs Manager
PPD, part of Thermo Fisher Scientific
- Rina has more than 10 years of experience in Regulatory Affairs and she is the Subject Matter Expert for the EU Clinical Trial Regulation 536/2014.
- Rina is the Leader of several implementation initiatives of EUCTR, working cross departmentally in order to align tasks, interactions, roles and responsibilities.
- Rina wrote the guidance for EUCTR super users, for the redaction process and the SOP aligning the different roles responsible for the CTA submission
Disclosure information not submitted.
Be ready for EU CTR: Strategy, Systems and Lessons Learned
Wednesday, May 10, 2023
08:00 – 16:00 CEST