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v platném znění
as amended

1084/ 2003 v platném znění.
at the end of the mutual recognition procedure there was a discrepancy between different eu member states regarding the wording of the indication that should adequately reflect the clinical data submitted by the company, and an official referral for arbitration according to article 6(12) of commission regulation ec no 1084/ 2003, as amended, was notified by belgium to the chmp on 19 october 2007.

1084/ 2003, v platném znění.
at the end of the mrp procedure there was a discrepancy between different member states regarding the wording of the indication that adequately reflects the clinical data submitted by the company, and an official referral for arbitration according to article 6(12) of commission regulation ec no 1084/ 2003, as amended, was notified by spain to the chmp on 1.12.2005.

st-1) v platném znění;
st-1), as they may be revised.

en iso 3405 v platném znění
en iso 3405 as amended

no 253/1957, v platném znění.
no 253/1957, as amended.

nr. 253/1957, v platném znění
no 253/1957, as amended

80/ 217/ ehs v platném znění).
authorisation holder is pfizer ltd.

bs 2000 část 170 v platném znění
bs 2000 part 170 as amended

i no 38/1999, v platném znění.
i no 38/1999, as amended.

l 147, s. 1) v platném znění.
1), in the currently applicable version.

i nr. 203/1999, v platném znění
i no 203/1999, as amended

: nařízení komise (v platném znění).
: commission’s regulations (a same nd ed ).

2 směrnice 2001/ 83, v platném znění.
as these concerns were not resolved during the course of the procedure, and since the 90mg dose of etoricoxib was used in both ra and as, a notification of an official referral for arbitration under article 31(2) of directive 2001/ 83, as amended to the chmp was made by france on 19 september 2007.

směrnice 91/414/ehs v platném znění.
directive 91/414/eec as amended.

4 směrnice 2001/ 82/ es v platném znění.
2 article 36(4) of directive 2001/82/ec, as amended

2 směrnice 2001/ 82/ es, v platném znění.
as the procedure concerns a range of products, the assessment has been limited to specific parts of the authorisations in accordance with article 35(2) of directive 2001/ 82/ ec, as amended.

16/ 17 rady 80/ 217/ ehs, v platném znění).
16/ 17 the import, sale, supply and/ or use of this veterinary medicinal product is only allowed under the particular conditions established by european community legislation on the control of csf (council directive 80/ 217/ eec, as amended).

ii směrnice rady 96/49/es v platném znění.
all derogations, restrictions and exemptions are also listed in section ii of the council directive 96/49/ec in its valid version.

sbírka zákonů č. 5, položka 34 v platném znění.
oj no 5 (34) as amended.