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Official Journal of the European Union
5.2.2013
COMMISSION IMPLEMENTING REGULATION (EU) No 103/2013
of 4 February 2013
amending Regulation (EC) No 786/2007 as regards the name of the holder of the authorisation of a
preparation of endo-1,4-beta-mannanase EC 3.2.1.78 (Hemicell)
(Text with EEA relevance)
THE EUROPEAN COMMISSION,
(4) To
allow
Eli
Lilly
and
Company
Ltd
to
exploit
its
marketing rights it is necessary to change the terms of
Having regard to the Treaty on the Functioning of the European
the authorisation.
Union,
(5) Regulation
(EC)
No
786/2007
should
therefore
be
amended accordingly.
Having regard to Regulation (EC) No 1831/2003 of the
European Parliament and of the Council of 22 September
(6)
Since safety reasons do not require the immediate appli
2003 on additives for use in animal nutrition ( 1 ) and in
cation of the amendment made by this Regulation to
particular Article 13(3) thereof,
Regulation (EC) No 786/2007, it is appropriate to
provide for a transitional period during which existing
Whereas:
stocks may be used up.
(7) The
measures
provided
for
in
this
Regulation
are
in
(1) ChemGen
Corp.
has
submitted
an
application
under
accordance with the opinion of the Standing
Article 13(3) of Regulation (EC) No 1831/2003
Committee on the Food Chain and Animal Health,
proposing to change the name of the holder of the auth
orisation as regards Commission Regulation (EC) No
HAS ADOPTED THIS REGULATION:
786/2007 ( 2 ) concerning the 10 year authorisation of a
preparation of endo-1,4-beta-mannanase EC 3.2.1.78
Article 1
(Hemicell), belonging to the additive category ‘zoo
technical additives’ and to the functional group ‘digesti
In column 2 of the Annex to Regulation (EC) No 786/2007 the
bility enhancers’.
words ‘ChemGen Corp., represented by Disproquima S.L.’ are
replaced by ‘Eli Lilly and Company Ltd’.
(2) The
applicant
claims
that,
with
effect
from
10
February
Article 2
2012, ChemGen Corp. was acquired by Eli Lilly and
Company Ltd which now owns the marketing rights
Existing stocks of the additive which are in conformity with the
for that additive. The applicant has submitted relevant
provisions applying before the date of entry into force of this
data supporting its request.
Regulation may continue to be placed on the market and used
until they are exhausted.
(3)
The proposed change of the terms of the authorisation is
Article 3
purely administrative in nature and does not entail a
fresh assessment of the additive concerned. The
This Regulation shall enter into force on the twentieth day
European Food Safety Authority was informed of the
following that of its publication in the Official Journal of the
application.
European Union.
This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 4 February 2013.
For the Commission
The President
José Manuel BARROSO
( 1 ) OJ L 268, 18.10.2003, p. 29.
( 2 ) OJ L 175, 5.7.2007, p. 8.

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