Regulatory Affairs Certificate
発行日 02/2014 • 有効期限 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.
Desired delivery: before 2025年6月1日
Manufacturer: China Medical IVD Product Manager Ltd., China
Lead time: 7 days
Desired delivery: before 2025年6月1日
Manufacturer: India Lab Scientific Advisory Pvt. Ltd., India
Lead time: 21 days