Martie van Heerden

Martie holds extensive regulatory knowledge spanning various product categories and therapeutic fields, and encompassing prescription and OTC medicines as well as medical devices.

Martie held multiple roles in the South African regulatory sector, which gradually expanded to encompass regulatory work across various African territories. Since relocating to New Zealand, Martie has been involved in a variety of applications submitted to TGA (Australia) and Medsafe (New Zealand), including exemption requests, provisional determinations, orphan drug applications, and GMP clearances, among others.