INC9 REPORT.pdf - Rotterdam Convention
INC9 REPORT.pdf - Rotterdam Convention
INC9 REPORT.pdf - Rotterdam Convention
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UNEP/FAO/PIC/INC.9/21<br />
regulatory action was taken as a consequence of a risk evaluation of the anticipated or likely uses of the<br />
chemical in the notifying country. The Committee agreed that the extent to which notifications and<br />
supporting documentation were found to meet the criteria in Annex II of the <strong>Convention</strong> would need to be<br />
considered on a case-by-case basis.<br />
71. The Committee recognized the right of any country to take domestic regulation action regarding use<br />
of chemicals and recalled that that action must be notified under the terms of the <strong>Convention</strong>.<br />
72. The Committee considered the three main scenarios concerning the ability of countries to provide<br />
risk evaluations in support of final regulatory actions. It was stressed that, even when hazard or risk<br />
evaluation information was taken from another country, supporting documentation would be expected to<br />
demonstrate that conditions in that country were similar and comparable to those in the notifying country.<br />
The supporting documentation could include “bridging” information on, among others things, a comparison<br />
of uses, conditions of use, physical and climatic conditions and risk reduction measures. The level of detail<br />
of that information should be sufficient to enable the Interim Chemical Review Committee to judge whether<br />
conditions were comparable. Further, the sufficiency and acceptability of that information would have to be<br />
determined by the Interim Chemical Review Committee on a case-by-case basis.<br />
73. The Committee noted that, in the absence of documentation detailing how the risk evaluation used<br />
from another country related to conditions prevalent in the notifying country, such an action would not be<br />
considered as meeting the criteria of Annex II of the <strong>Convention</strong>.<br />
74. The Committee requested the Interim Chemical Review Committee to develop guidelines on the<br />
scope of “bridging” information to be contained in the supporting documentation provided by the notifying<br />
country, for review by the Committee at its tenth session.<br />
75. The Committee noted the concern of developing countries with regard to the need to avoid overburdening<br />
developing countries with requirements to provide extensive amounts of information.<br />
2. Issues to consider in ensuring consistency between the scope of reported national regulatory<br />
actions and the inclusion of the chemical in the interim prior informed consent procedure<br />
76. The Committee had before it the documentation prepared for the subject (see annex I). Introducing<br />
the sub-item, Mr. Arndt, Chair of the Interim Chemical Review Committee, pointed to the inconsistent use<br />
of chemical abstract (CAS) numbers and chemical descriptions in Annex III of the <strong>Convention</strong>. He drew the<br />
Committee’s attention to the Review Committee’s request for guidance on ensuring consistency between the<br />
scope of reported national regulatory actions and the listing of chemicals in the interim PIC procedure, as set<br />
forth in document UNEP/FAO/PIC/INC.9/9.<br />
77. The Committee noted that the scope of the regulatory actions as stated in the notifications submitted<br />
in accordance with Article 5 was the basis for listing a given chemical. The Committee agreed that, in the<br />
case of a chemical such as DNOC, it would be listed as “DNOC and its salts, such as ammonium salt,<br />
potassium salt and sodium salt”, along with the relevant CAS numbers, if included in the interim PIC<br />
procedure.<br />
78. The Committee noted that the specific formulation identified in a proposal submitted in accordance<br />
with Article 6 was the basis for listing a severely hazardous pesticide formulation. The Committee agreed<br />
that formulations containing the active ingredient or ingredients at or above the specified concentrations and<br />
in the same formulation type would also be subject to the interim PIC procedure, if supported by the<br />
technical documentation supporting the proposal. It was agreed that a footnote to that effect could be added,<br />
or some other type of explanatory guidance could be provided.<br />
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