A package of new and updated guidance on licensing and certification processes for manufacturers of medicines and biologicals in Australia, has been developed in consultation with the Therapeutic Goods Administration (TGA) Industry Working Group on GMP (TIWGG), to better support manufacturers and sponsors and provide additional clarity for applicants.
The new guidance does not introduce changes to the current process or requirements, existing processes have merely been documented with additional clarity.
The updated package of guidance was published in August 2017 and is now available on the TGA website, on the Manufacturing Therapeutic Goods pages.
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