Regulatory Affairs Certificate
颁发日期 02/2014 • 到期日期 02/2020
KFDA registration expert with expertise in Korean pharmaceutical regulatory requirements. Experienced in KGMP certification and bioequivalence study review. Specialist in Korean language dossier preparation.
期望交付: 早于 2025年6月1日
Manufacturer: China Medical IVD Product Manager Ltd., China
交付周期: 7 天
期望交付: 早于 2025年6月1日
Manufacturer: India Lab Scientific Advisory Pvt. Ltd., India
交付周期: 21 天