Regulatory Documentation

Access guidance documents on tissue banks, standing databases, and clinical research regulations. Always check your institution's latest policies, as some articles may be outdated.

Last updated 7 August 2026

Chicken Soup Series - Regulatory Documentation

(May 2022) How to Handle Leftover Tissues for Future Unapproved Research and Legacy Human Biological Material (LHBM) (opens in new tab)
(Dec 2021) When and How to Register for a Standing Database (opens in new tab)
(Jan 2020) How to Set Up a Tissue Bank? (opens in new tab)
(Jul 2019) Clinical Research Material (CRM) notification for Clinical Research involving Medical Devices (opens in new tab)

Learn more about the regulatory overview of Clinical Trials by Health Sciences Authority (HSA) here (opens in new tab).

_DISCLAIMER_{: Past Issues/Articles may contain best practices, policies or SOPs that have been superseded or may no longer relevant or applicable. For NHG Health and partner institutions, we encourage you to refer to the latest NHG Health PCR SOPs (available via NHG Health Intranet access or Partner Institution’s CRU/Research office). Always refer to your own institution’s latest policy, SOPs, guidance documents and templates.}