Regulatory – All regulatory activities are handled in-house, including all TGA submissions and approvals. Our regulatory department has a wide range of knowledge and experience with medicines, cosmetics, and devices. This involves dealing with applications for TGA and NICNAS. They are also involved in licensing and GMP applications. We are able to offer experience and advice for in-licensed brands as part of our business relationships.
All Key Pharmaceuticals brands comply with Australian and New Zealand regulatory requirements, where applicable.
Contract Manufacture – Key Pharmaceuticals manages a broad range of contract manufacturing relationships from full products, part products and also supply of components.
Packing – the company has an in-house secondary packing facility which complies with TGA, GMP and ISO requirements. When required, primary packaging is outsourced to GMP licensed contractors.
Release for sale – All products are released for sale by in-house quality assurance staff.
Warehousing – Key Pharmaceuticals has on-site warehousing facilities which include a temperature controlled environment and bar code printing facilities.