Regulatory Affairs Certificate
발급일 02/2014 • 만료일 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 2025년 6월 1일
Manufacturer: China Medical IVD Product Manager Ltd., China
Lead time: 7 days
Desired delivery: before 2025년 6월 1일
Manufacturer: India Lab Scientific Advisory Pvt. Ltd., India
Lead time: 21 days