Chenfang S.
In-house exp. - CMC/Clinical Trial/Regulatory Approval
Years of experience: 11
- English Chinese
-
China22:56
-
Rate per word €0.08 EUR
--- Background ---
- MA in Translation, 3 years as in-house translator at Novartis, experienced in regulatory submissions
- 7+ years working with CROs including IQVIA (Quintiles) and Tigermed
--- Services ---
- Regulatory documentation - CMC, clinical trial, PK & PD, safety, protocols, IB, CSR, site audit, FDA inspection, ICF, etc.
- Marketing content for healthcare professionals - brochures, websites, ebooks, presentations, etc.
- IFUs of drugs and medical devices
- MA in Translation, 3 years as in-house translator at Novartis, experienced in regulatory submissions
- 7+ years working with CROs including IQVIA (Quintiles) and Tigermed
--- Services ---
- Regulatory documentation - CMC, clinical trial, PK & PD, safety, protocols, IB, CSR, site audit, FDA inspection, ICF, etc.
- Marketing content for healthcare professionals - brochures, websites, ebooks, presentations, etc.
- IFUs of drugs and medical devices
Translated content of:
Language variants:
- Source languages
- English – US
- Target languages
- Chinese – Simplified
Credentials: