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Section 38A - Therapeutic Goods Act 1989 - Guidelines for multi‑site licences | Zoe

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Therapeutic Goods Act 1989

38AGuidelines for multi‑site licences

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38A Guidelines for multi‑site licences

The Secretary must, by legislative instrument, make guidelines setting out the circumstances in which a licence may cover 2 or more manufacturing sites.

Previous section38Grant of licence

Next section38BSplitting multi‑site licences