News
September 17, 2018

New Zealand set to increase fees

New Zealand set to increase fees for Hazardous Substance and new organisms import and approval applications.
August 15, 2018

GMP Clearance for Complementary Products

Even for low-risk complementary medicine products, GMP (Good Manufacturing Practice) clearance is required.
July 12, 2018

Avoid these pitfalls with 5 Batch Analysis

A 5 batch analysis report is a requirement for the regulatory approval of a chemical active ingredient with the APVMA and indeed by most global regulatory bodies.