Regulatory Affairs Certificate
発行日 07/2020 • 有効期限 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 2025年6月1日
Manufacturer: Belgium Pharma Customs Specialists BVBA, Cyprus
Lead time: 21 days
Desired delivery: before 2025年6月1日