The information in this document is provided for guidance only. It should not be relied on to address every aspect of the relevant legislation. You should seek your own independent legal advice to ensure that all of the legal requirements are met.
It is a legal requirement for sponsors of therapeutic goods supplied under the Special Access Scheme (SAS) and Authorised Prescriber (AP) scheme to provide six monthly reports to the Secretary of the Therapeutic Goods Administration (TGA) under paragraph 47B(1)(c) of the Therapeutic Goods Regulations 1990.