Australia: release of therapeutic goods for supply
26/6/2011
Presented at: RACI seminar 'Release of Therapeutic Goods (Human and Vet) for Supply in Australia', 26 May 2011
Summary: The seminar program included presentations on Release for Supply of human and veterinary medicines by the TGA and APVMA respectively.
This presentation provides an overview of the requirements under the Manufacturing Principles for release for supply, the differentiation between release for sale and release for supply and of partially and fully finished products, the responsibilities of the parties involved, the assessment process and evidence used for release and the changes to the Manufacturing principles that have impacted on release for supply.
A number of Answers were provided to Questions received from participants prior to the seminar.
This presentation is provided for informational purposes only and is not intended to define specific requirements for regulatory submissions or for achieving compliance to manufacturing standards for Release for Supply.
Author: Greer Deal, Director of Global Regulatory Services (GRS)