Good Regulatory Practices and Technical Competencies

This workshop will provide an exchange of information and capacity building between the South African Health Products Regulatory Authority, SAPHRA and partner reference NRAs including the WHO, USFDA, TGA, HSA, ANVISA, covering the core international references for medical device regulatory. The workshop objective is to support and advance to strengthen the soft infrastructure of medical device regulatory framework to incorporate global lessons learned from the COVID-19 pandemic, to better prepare for future health emergencies, to prevent the implementation of unnecessary regulatory barriers to medical technologies, to improve general MD NRA public administration and general public health.

Date: 14 November 2023
Time: 9:00 – 17:30 Pretoria, South Africa (2:00 am – 10:30 ET)
Platform: Hybrid (In-person: Southern Sun Pretoria Hotel, Cnr. Steve Biko and, Pretorius St, Arcadia, Pretoria, 0083). Please register here for virtual or in-person participation.