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Health Sciences Authority

Regulatory Requirements for Clinical Research Materials

Learn the regulatory requirements for Clinical Research Materials.

Last updated on 31 October 2026

This module on the regulatory requirements for Clinical Research Materials covers the following:

  • Clinical Research Materials (CRM)

  • Objectives of the CRM Regulations

  • CRM Notification

  • Duties and Responsibilities of Local Manufacturers, Importers and Suppliers of CRM

Version date: 28 Jul 2025
(Click here to download the slide deck [PDF, 439 KB] (opens in new tab))

Thumbnail for IOCTB Learn - Regulatory Requirements for Clinical Research Materials

Note: With effect from 1 Nov 2026,

  • The Innovation Office and Clinical Trials Branch (IOCTB) will be renamed Investigational Medicines and Non-Clinical Assessments Division (IMNAD).

  • IOCTB Learn will be renamed Clinical Trials Learn. Previously published slides and videos will retain the former names.