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Health Sciences Authority

IOCTB Learn

Clinical Trials Learning and Educational Hub.

Last updated 23 March 2026

Welcome to IOCTB Learn, a clinical trials learning and educational hub to support sponsors, investigators and clinical research professionals in understanding Singapore’s regulatory requirements for clinical trials and Good Clinical Practice (GCP). This flexible, self-paced learning approach allows you to access these educational resources at your convenience, helping you to enhance the quality and integrity of clinical trials conducted in Singapore.

Disclaimer: Please note that the presentations (including videos) are intended to provide general guidance. Although we have tried to ensure that the information contained within them is accurate, we do not, however, warrant their accuracy or completeness.

The Health Sciences Authority (HSA) accepts no liability for any errors or omissions in presentations, or for any action / decision taken or not taken as a result of using the information contained therein. If you need specific legal or professional advice, you should consult your own legal or other relevant professional advisers. In the event of any contradiction between the contents of the presentations and any written law, the latter should take precedence.

The presentations and all content within them including without limitation, images, video clips, writing and logos, belong to the Health Sciences Authority (HSA). You may view the presentations for internal reference only, but otherwise, no part of the content in the presentations may be copied, used, reproduced, extracted or modified by you, without the prior written approval of HSA. HSA’s rights are expressly reserved.

Workshop on Sponsor Oversight of IITs

Learn what is required for sponsor oversight of Investigator-Initiated Trials (IITs).

Regulatory Requirements for Clinical Trials of TPs and Class 2 CTGTPs

Learn the regulatory requirements for clinical trials of Therapeutic Products and Class 2 Cell, Tissue and Gene Therapy Products.

Regulatory Requirements for Clinical Research Materials

Learn the regulatory requirements for Clinical Research Materials.

Expedited Safety Reporting Requirements for HSA Authorised/Notified Clinical Trials

Learn the expedited safety reporting requirements for HSA authorised / notified clinical trials.

Good Clinical Practice Inspections

Learn HSA’s Good Clinical Practice (GCP) inspection framework.

HSA-SCRI Webinar: ICH E6 (R3) Guideline for GCP - Principles and Annex 1

Webinar recording on major changes to ICH E6 (R3) Principles and Annex 1