Commission Implementing Regulation (EU) No 503/2013 of 3 April 2013 on applications for authorisation of genetically modified food and feed in accordance with Regulation (EC) No 1829/2003 of the European Parliament and of the Council and amending Commission Regulations (EC) No 641/2004 and (EC) No 1981/2006 (Text with EEA relevance) (c. 503)

ANNEX I U.K. PREPARATION AND PRESENTATION OF APPLICATIONS

PART VII U.K. SUMMARY OF APPLICATIONS

1. GENERAL INFORMATION U.K.

1.1. Details of application U.K.

(a) Member State of application U.K.

(b) Application number U.K.

(c) Name of the product (commercial and any other names) U.K.

(d) Date of acknowledgement of valid application U.K.

1.2. Applicant U.K.

(a) Name of applicant U.K.

(b) Address of applicant U.K.

(c) Name and address of the representative of the applicant established in the Union (if the applicant is not established in the Union) U.K.

1.3. Scope of the application U.K.

(a) Genetically modified food U.K.



Food containing or consisting of genetically modified plants



Food produced from genetically modified plants or containing ingredients produced from genetically modified plants

(b) Genetically modified feed U.K.



Feed containing or consisting of genetically modified plants



Feed produced from genetically modified plants

(c) Genetically modified plants for food and feed use U.K.



Products other than food and feed containing or consisting of genetically modified plants with the exception of cultivation



Seeds and plant propagating material for cultivation in the Union

1.4. Is the product or the uses of the associated plant protection product(s) already authorised or subject to another authorisation procedure within the Union? U.K.

No	
Yes		(in that case, specify)

1.5. Has the genetically modified plant been notified under Part B of Directive 2001/18/EC? U.K.

Yes	
No		(in that case, provide risk analysis data on the basis of the elements of Part B of Directive 2001/18/EC)

1.6. Has the genetically modified plant or derived products been previously notified for marketing in the Union under Part C of Directive 2001/18/EC? U.K.

No	
Yes		(in that case, specify)

1.7. Has the product been subject to an application and/or authorised in a third country either previously or simultaneously to this application? U.K.

No	
Yes		In that case, specify the third country, the date of application and, where available, a copy of the risk assessment conclusions, the date of the authorisation and the scope of the application

1.8. General description of the product U.K.

(a) Name of the recipient or parental plant and the intended function of the genetic modification U.K.

(b) Types of products planned to be placed on the market according to the authorisation applied for and any specific form in which the product must not be placed on the market (such as seeds, cut-flowers, vegetative parts) as a proposed condition of the authorisation applied for U.K.

(c) Intended use of the product and types of users U.K.

(d) Any specific instructions and recommendations for use, storage and handling, including mandatory restrictions proposed as a condition of the authorisation applied for U.K.

(e) If applicable, geographical areas within the Union to which the product is intended to be confined under the terms of the authorisation applied for U.K.

(f) Any type of environment to which the product is unsuited U.K.

(g) Any proposed packaging requirements U.K.

(h) Any proposed labelling requirements in addition to those required by other applicable EU legislation than Regulation (EC) No 1829/2003 and when necessary a proposal for specific labelling in accordance with Article 13(2) and (3), Article 25(2)(c) and (d) and Article 25(3) of Regulation (EC) No 1829/2003 U.K.

In the case of products other than food and feed containing or consisting of genetically modified plants, a proposal for labelling which complies with the requirements of point A(8) of Annex IV to Directive 2001/18/EC must be included.

(i) Estimated potential demand U.K.

(i)

In the EU

(ii)

In EU export markets

(j) Unique identifier in accordance with Regulation (EC) No 65/2004. U.K.

1.9. Measures suggested by the applicant to take in the case of unintended release or misuse of the product as well as measures for its disposal and treatment U.K.