
Article 1 
Annex III to Regulation (EC) No 853/2004 is amended in accordance with the Annex to this Regulation.
Article 2 
This Regulation shall enter into force on the 20th day following its publication in the Official Journal of the European Union.
This Regulation shall be binding in its entirety and directly applicable in all Member States.Done at Brussels, 24 October 2007.
For the Commission
Markos KYPRIANOU
Member of the Commission
ANNEX

Annex III to Regulation (EC) No 853/2004 is amended as follows:

1.. in point 3 of Section VIII, the following paragraph is added:
'By way of derogation from point (a), point 7 of Part A of Annex I to Regulation (EC) No 852/2004 may not apply to operators engaged in small-scale coastal fishing within the meaning of Article 26(1) of Council Regulation (EC) No 1198/2006, and carrying out their activities only for short periods of less than 24 hours.';
2.. in Section XIV, Chapters III, IV and V are replaced by the following:
'
CHAPTER III:  1. 

((a)) all ruminant bone material derived from animals born, reared or slaughtered in countries or regions with a controlled or undetermined BSE risk in accordance with Community legislation is subjected to a process which ensures that all bone material is finely crushed and degreased with hot water and treated with dilute hydrochloric acid (at minimum concentration of 4 % and pH < 1,5) over a period of at least two days. This treatment is followed either by:

— an alkaline treatment of saturated lime solution (pH > 12,5) for a period of at least 20 days with a heat treatment step of 138 °C minimum during at least four seconds, or
— an acid treatment (pH < 3,5) during 10 hours minimum with a heat treatment step of 138 °C minimum during at least four seconds, or
— a heat-and-pressure process for at least 20 minutes with saturated steam of 133 °C at more than 3 bars, or
— any approved equivalent process;
((b)) other raw material is subjected to a treatment with acid or alkali, followed by one or more rinses. The pH must be adjusted subsequently. Gelatine must be extracted by heating one or more times in succession, followed by purification by means of filtration and heat treatment.
 2. A food business operator may produce and store both gelatine intended for human consumption and gelatine not intended for human consumption in the same establishment provided that the raw materials and the production process comply with the requirements applying to gelatine intended for human consumption.

CHAPTER IV: 
Food business operators must ensure that gelatine complies with the residue limits set out in the following table:


Residue Limit
As 1 ppm
Pb 5 ppm
Cd 0,5 ppm
Hg 0,15 ppm
Cr 10 ppm
Cu 30 ppm
Zn 50 ppm
SO2 (European Pharmacopoeia 2005) 50 ppm
H2O2 (European Pharmacopoeia 2005) 10 ppm

CHAPTER V: 
Wrapping and packaging containing gelatine must bear the words “gelatine fit for human consumption” and must indicate the date of minimum durability.
';
3.. in Section XV, Chapter III, point 3 is replaced by the following:
'
3. A food business operator may produce and store both collagen intended for human consumption and collagen not intended for human consumption in the same establishment provided that the raw materials and the production process comply with the requirements applying to collagen intended for human consumption.
';
4.. the Appendix is replaced by the following:

‘Appendix to ANNEX III 
Number of the commercial document: …
 I. 
Nature of the raw material: …

Animal species: …

Type of packaging: …

Number of packages: …

Net weight (kg): …
 II. 
Type, name, address and approval/registration/special authorisation number of the establishment of origin:

…

Name and address of the consignor: …
 III. 
Type, name, address and approval/registration/special authorisation number of the production establishment of destination:

…

Name and address of the consignee: …
 IV. Means of transport: …

Done at …, on …

…

(Signature of the operator of the establishment of origin or its representatives)

