CHAPTER II

ACTIVE SUBSTANCES, SAFENERS, SYNERGISTS AND CO-FORMULANTS
SECTION 4

Registers

Approvals register
Article 27A
1
The competent authorities must jointly establish and maintain a register of active substances, safeners, synergists, low-risk active substances, basic substances and candidates for substitution approved in accordance with this Regulation.
2
The entry on the register for each substance must contain the following information—
a
the common name and identification numbers of the substance;
b
the IUPAC name of the substance, where available;
c
the minimum purity of the substance;
d
in respect of each constituent territory to which the entry relates—
i)
whether the substance has been approved as an active substance, safener, synergist, low-risk active substance, basic substance or candidate for substitution;
ii)
the date of the approval decision;
iii)
except in relation to approved basic substances, the expiration date of approval;
iv)
information on any specific provisions, conditions or requirements in respect of the approved substance.
3
The register must contain a search facility.
4
The competent authorities must jointly make the register available for inspection by the public on a website maintained by one or more of the competent authorities.

Unacceptable co-formulants register
Article 27B
1
The competent authorities must jointly establish and maintain a register of co-formulants which are not acceptable for inclusion in a plant protection product in accordance with Article 27.
2
The entry on the register for each co-formulant must contain the following information—
a
the common name of the co-formulant;
b
the IUPAC name of the co-formulant (where available);
c
the CAS number of the co-formulant (where available);
d
the EC number of the co-formulant (where available);
e
in respect of each constituent territory to which the entry relates—
i)
the date of the decision that the co-formulant was not acceptable for inclusion in a plant protection product;
ii)
the sunset date for the co-formulant;
iii)
any conditions of restriction relating to the co-formulant;
iv)
any other information regarding the co-formulant that the competent authority considers relevant.
3
The register must contain a search facility.
4
The competent authorities must jointly make the register available for inspection by the public on a website maintained by one or more of the competent authorities.
Ch. 2 Section 4 inserted (31.12.2020) by The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 (S.I. 2019/556), regs. 1(1), 4(35) (with Sch. 1); 2020 c. 1, Sch. 5 para. 1(1)