Compiles and manages regulatory applications for Ferring products to health authorities, which includes new products, product dosage forms, indication. As well as registration maintenance through renewals & variations submissions.
Provides labelling support and maintaining SPC update in the region. Reviews locally prepared labelling before approval & implementation.
Ensures the availability and/or prepares regulatory documents and certificates for obtaining rapid approvals.
Reviews promotional materials developed by the marketing department from a regulatory point of view
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