Regulatory Affairs Certificate
발급일 07/2018 • 만료일 07/2024
NMPA registration specialist with expertise in Chinese pharmaceutical regulatory requirements. Experienced in CTD preparation for Chinese market. Specialist in clinical trial applications in China.
Lead time: 21 days
Desired delivery: before 2025년 6월 1일
Desired delivery: before 2025년 6월 1일
Manufacturer: Malaysia Pharma Quality Control Sdn. Bhd., Malaysia
Lead time: 21 days