Regulatory Affairs Certificate
발급일 07/2020 • 만료일 07/2026
EU MDR compliance lead with expertise in medical device regulatory transition. Experienced in technical documentation update and EUDAMED registration. Specialist in UDI implementation.
Manufacturer: Colombia Pharma Clinical Trial Coordinator S.A.S., India
Lead time: 14 days
Desired delivery: before 2025년 6월 1일
Manufacturer: Belgium Pharma Customs Specialists BVBA, Cyprus
Lead time: 21 days
Desired delivery: before 2025년 6월 1일