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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 926 to 950
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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
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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 Non response to a s41JA, effective 26/01/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 26/01/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 26/01/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 26/01/2021
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion and and a certification made under 41FD(e) is incorrect in a material particular, effective 26/01/2021
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Cancellation or suspensionRegulatory action due to Non response to s41JA, effective 25/01/2021
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, non- response to a s41JA, the safety and performance of the kind of Device is unacceptable and a certification made under 41FD(f) is incorrect in a material particular, effective 22/01/2021
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Cancellation or suspensionRegulatory action due to The certification under paragraph 26A(2)(ja) is incorrect (paragraph 30(2)(ba) of the Act).The presentation of the listed goods is unacceptable (paragraph 30(2)(aa) of the Act).The goods do not conform to a requirement relating to advertising applicable to the goods under Part 5-1 or the regulations (paragraph 30(2)(ea) of the Act)., effective 22/01/2021
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 22/01/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 21/01/2021
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Cancellation or suspensionRegulatory action due to The certification under paragraphs 26A(2)(j) and 26A(2)(ja) of the Act is incorrect (paragraph 30(2)(ba) of the Act).The presentation of the listed goods is unacceptable (paragraph 30(2)(aa) of the Act)., effective 15/01/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 14/01/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 14/01/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 14/01/2021
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/01/2021