Complementary Medicines – Use of the ZA-CTD format in the preparation of registration applications

This guideline is intended to provide recommendations to applicants wishing to submit applications for the registration of Complementary Medicines intends to invite comment from all stakeholders with the view to present Pro ducts Regulatory Authority (SAHPRA) for authori s ation. In addition to this guideline, the Authority to the South African Health reserves the right to request any additional in formation to establish the safety, quality and efficacy of a medicine in keeping with the knowledge current time of evaluation. The SAHPRA at the is committed to ensure that all registered medicines will be of the required quality, safety and efficacy Gu . idelines and application forms are available from the First publication for comment SAHPRA website: www.sahpra.org.za

2020 Jun