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Posted 15/10/2024 by CK Group- Science, Clinical and Technical
Supports the EMEA Regulatory Affairs team for post-approval activities for MRP/DCP products across EEA and coordinate worksharing (WS) procedures for CMC and non-CMC variation, when WS is appropriate. Development of regulatory strategies, preparation of regulatory applications and … more
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Posted a week ago by SRG
Completes the intake process of complaints through phone and email into the Complaint Intake Systems which includes translations from local language to English when required, the initial identification of the complaint code, conducting follow up activities for missing information, coordinating</ … more
