Regulatory Affairs Certificate
発行日 09/2018 • 有効期限 09/2024
Regulatory affairs director with expertise in EU MDR and IVDR compliance. Experienced in notified body interactions and technical file preparation. Specialist in clinical evaluation reports.
Buyer: Indian Vaccines Development Director Pvt. Ltd., India
Lead time: 60 days
Desired delivery: before 2025年10月1日
Manufacturer: India Freight Distribution Center Pvt. Ltd., India
Lead time: 90 days
Distributor: Indian Vaccines Development Director Pvt. Ltd., India
Desired delivery: before 2025年10月1日