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Purpose
Facilitate regulatory and ethics engagement in an agenda that is mutually beneficial to the advancement of clinical trials in South Africa.
Objectives
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Contribute to continuous improvement in Regulatory and Ethical compliance environment that enables clinical research development in South Africa.
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Collaborate with various stakeholders to ensure seamless conduct of clinical trials in South Africa.
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Engage stakeholder - quicker/response/ turn around - Implementation of new guidelines.
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Involved in the development of guidelines ensuring appropriate sector input.
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Represent members in regulatory decision making.
Information HUB

SAHPRA

Clinical Trials
Registry

Clinical Trials
Ethics in South Africa

South African Good Clinical Practice
Regulatory Platforms

Upcoming Events
Import/Export Permit Process in collab with DOH
04 Mar | 09:00
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INFORMATION
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