Risk management plan (RMP)
Find out the RMP requirements for therapeutic products and cell, tissue or gene therapy products (CTGTP) registered in Singapore.
Last updated on 17 March 2026
Overview on RMP
Understand the components of an RMP and their role in addressing risks associated with a product.
RMP submission for product registration
Find out when an RMP submission is required and the documents to be submitted.
Post-registration RMP obligations
Understand your RMP obligations as registrants of therapeutic products and CTGTP.