Regulatory Documentation

Chicken Soup Series - Regulatory Documentation

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

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

_DISCLAIMER_{: Past Issues/Articles may contain best practices, policies or SOPs that have been superseded or may no longer relevant or applicable.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