- Proofread translated labels by checking the correctness of the translation, spelling, grammar, text completeness, and storage conditions.
- Perform regulatory review and local adaptation of translated labels according to local regulatory requirements.
- Execute proofreading and regulatory review of label printouts.
- Approve documents by signing each page.
- Provide regulatory consulting on clinical trial related aspects including medicines, devices, and IVDs.
- Manage interactions with Health Authorities where applicable.