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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 701 to 725
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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 29/07/2021
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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 29/07/2021
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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 29/07/2021
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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 29/07/2021
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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 29/07/2021
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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 29/07/2021
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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 29/07/2021
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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 29/07/2021
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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 29/07/2021
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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 29/07/2021
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Cancellation or suspensionRegulatory action due to Under subsection 41GA(1)(b); it is likely that there are grounds for cancelling this kind of device from the ARTG under subsection 41GN(1)(b) & (1)(e)., effective 28/07/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 27/07/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 27/07/2021
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Cancellation or suspensionRegulatory action due to The presentation of the listed goods is unacceptable (paragraph 30(2)(aa) of the Act).The certification under paragraph 26A(2)(ja) of the Act is incorrect (paragraph 30(2)(ba) of the Act)., effective 23/07/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 22/07/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 22/07/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 22/07/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 22/07/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 22/07/2021
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Cancellation or suspensionRegulatory action due to Nonresponse to a s41JA, effective 22/07/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/07/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/07/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/07/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/07/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/07/2021