Regulatory affairs: Clinical trial applications & product registrationBELTAS 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.
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"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 |
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