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COMMONWEALTHRegulation
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s 8AK

Information to be given in notice to holder

In force
Part 1Preliminary
Division 1.3General provisions about notices

8AK Information to be given in notice to holder

For paragraph 8F(2)(e) of the Code, the following information is prescribed for a notice given to a holder under subsection 8F(1) of the Code:

(a)

for the approval of an active constituent:

(i)

the information required by section 8H of the Code in relation to the approval; and

(ii)

the date of the approval under section 22 of the Code; and

(iii)

the date on which the notice is given to the holder; and

(iv)

any other details entered in the Record about the active constituent that the APVMA thinks appropriate;

(b)

for the registration of a chemical product:

(i)

the information required by section 8H of the Code in relation to the registration; and

(ii)

the date of the registration under section 22 of the Code; and

(iii)

the distinguishing name of the chemical product; and

(iv)

the date on which the notice is given to the holder; and

(v)

any other details about the chemical product, entered in the Register, that the APVMA thinks appropriate;

(c)

for the approval of a label:

(i)

the date of the approval under section 22 of the Code; and

(ii)

the distinguishing number of the label; and

(iii)

the date on which the notice is given to the holder; and

(iv)

any other details about the label, entered in the relevant APVMA file, that the APVMA thinks appropriate;

(d)

for the variation of a relevant particular or condition:

(i)

the information required by section 8J of the Code in relation to the variation; and

(ii)

the date of the variation under section 22 of the Code; and

(iii)

the date on which the notice is given to the holder; and

(iv)

for a variation of a relevant particular or condition of an approval of an active constituent—any other details entered in the Record about the active constituent that the APVMA thinks appropriate; and

(v)

for a variation of a relevant particular or condition of a registration of a chemical product—any other details about the chemical product, entered in the Register, that the APVMA thinks appropriate; and

(vi)

for a variation of a relevant particular or condition of an approval of a label—any other details about the label, entered in the relevant APVMA file, that the APVMA thinks appropriate.

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