Regulatory Affairs Certificate
颁发日期 07/2020 • 到期日期 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
交付周期: 14 天
期望交付: 早于 2025年6月1日
Manufacturer: Belgium Pharma Customs Specialists BVBA, Cyprus
交付周期: 21 天
期望交付: 早于 2025年6月1日