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Action
- Medical device cancellation (827)
- Medicine suspension (472)
- Complementary medicine cancellation (203)
- Medical device suspension (86)
- Medicine cancellation (59)
- Revocation of a TGA issued Conformity Assessment Certificate (51)
- Medical device cancellation - certain devices within an entry (22)
- Registered medicine cancellation (12)
- Voluntary revocation at the request of the manufacturer (9)
- Medical device cancellation - requested by the sponsor - certain devices within an entry (8)
- Medical device cancellation (7)
- Listed medicine cancellation (3)
- Listed medicine cancellation (3)
- Revocation of a TGA issued Conformity Assessment Certificate. (3)
- Revocation of medical device suspension (2)
- Revoked medicine suspension (2)
- Medical device cancellation (1)
- Medical device cancellation – certain devices within an entry (1)
- Suspension from the ARTG under subsection s41GA(1)(b) (1)
- Voluntary revocation at the request of the manufacturer. (1)
Find out more about Cancellations and Suspensions.
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1780 result(s) found, displaying 851 to 875
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 08/02/2021
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Cancellation or suspensionRegulatory action due to Incomplete response to a s41JA, effective 08/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 08/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a section 41JA, effective 05/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a section 41JA, effective 05/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a section 41JA, effective 05/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a section 41JA, effective 05/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a section 41JA, effective 05/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a section 41JA, effective 05/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a section 41JA, effective 05/02/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 03/02/2021
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 29/01/2021
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 29/01/2021
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 29/01/2021
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 29/01/2021
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 29/01/2021
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 29/01/2021
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 29/01/2021
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Cancellation or suspensionRegulatory action due to Under subsection 29D(1)(b); it is likely there are grounds for cancelling this medicine from the ARTG under section 30(2)(a) on the basis that the quality of the goods is unacceptable., effective 29/01/2021