Regulatory affairs: Clinical trial applications & product registration

BELTAS manages submissions in compliance with local regulations, both clinical trial applications and product registration.

We are familiar in dealing with regulatory authorities - Medsafe in New Zealand, the Therapeutic Goods Agency (TGA) in Australia, and a number of the European regulatory authorities.

"Patient recruitment consumes more time than any other clinical trial activity, with thirty per cent of clinical trial time spent finding and enrolling study subjects"

- Cutting Edge Information