154x Filetype DOCX File size 0.11 MB Source: www.hse.gov.uk
Application Form CRD2 Submission under Regulation (EC) No 1107/2009 Commercial authorisation of a plant protection product via the Administrative Stream where no technical assessment/data evaluation is required. When not to use this form Applications for: New commercial authorisation or new permit for trial purposes (use form CRD1). Extension of authorisation for minor use (use form CRD3). Official Listing of an Adjuvant (use form CRD4). Administrative permit for trial purposes (use form CRD7). Standalone Technical Equivalence (use form CRD8). Emergency authorisations under Article 53 (use form CRD9). Pre-submission meeting (use CRD10). Renewal of an existing plant protection product (use form CRD-R). Biocidal product authorisation (see http://www.hse.gov.uk/biocides/index.htm). By Post: Applications Sift, Chemicals Regulation Division, Mallard House, Kings Pool, 3 Peasholme Green, York, YO1 7PX, UK Application submission By Email: applications@hse.gov.uk By ShareFile (cloud based file sharing system): Please request details of CRD’s ShareFile by emailing applications@hse.gov.uk CRD contact details Telephone: 020 3028 1101 (International: (+44) 20 3028 1101) Enquiries Email: CRDInformationManagement@hse.gov.uk Website: http://www.hse.gov.uk/CRD/ How to complete this form Complete all parts of the form relevant to your application. All correspondence and enquiries will be sent to the contact named in the applicant section (Part A) of this form unless otherwise informed. No sections of the form are protected. Take care not to delete or amend existing text. To check ‘tick boxes’, double click on the box, select ‘checked’ and press ‘ok’. ‘Copy and paste’ to add additional rows/tables where appropriate. For questions about this form, see CRD contact details above. All forms and supporting information must be submitted to applications@hse.gov.uk. Guidance on the applications process can be found in the Applicant Guide. Note if this application form is not fully completed your application may be rejected. 1 Form CRD2 Version 04/22 Part A – Applicant details 1 Application The Authorisation Holder submitted Consultancy/Third Party by: Applicant Contact name Title* contact Company details name Address Telephone Email Date I confirm that the information given in this application form is true to the best of my knowledge, information and belief. (tick to confirm) 2 Address for Contact name Title* invoicing Company name Address Telephone Email 3 Purchase order number (if needed) * for example; Mr, Mrs, Ms, Dr Using personal data HSE is under a legal duty to protect any personal information we collect and we will only use that information in accordance with the law, including the General Data Protection Regulation (GDPR) (Regulation (EU) 2016/679), the Data Protection Act 2018, the Freedom of Information Act 2000 and the Environmental Information Regulations 2004. We meet our obligations as part of UK Government to safeguard data and prevent any unauthorised access to it through use of technical, personnel and procedural controls. More details on Government security can be found on the Gov.UK Web site: https://www.gov.uk/government/collections/government-security. In order to carry out our functions and respond to enquiries effectively, we will sometimes need to share information with other government departments, the emergency services, law enforcement agencies, public authorities (such as local authorities and the Environment Agency) and organisations acting on our behalf. However, we will only do this where it is required or permitted by law. 2 Form CRD2 Version 04/22 Part B – Type of Application 4 How many products does this application apply to 4a Application for 1 product 4b Application for 15 or more products that can be processed as a ‘blanket amendment’ (complete Appendix (only applies to changes which do not require a new MAPP 1) number to be issued) 5 What type of application are you applying for 5a Authorisation of a new product identical to an EXISTING authorised ‘parent’ product (specify below) (known as a 'back-to-back' application) Existing ‘parent’ product MAPP number Notice of name Authorisation Number 5b Authorisation of a new product identical to ONGOING applic- ation for a ‘parent’ product (specify below) (known as a 'back-to-back' application) Product name MAPP number ongoing COP number 5c Change in product tradename complete section G 5d Change in Authorisation Holder complete section G 5e Change in Marketing Company complete section G 5f Changes to authorised product identical to those considered for another authorised product 5g Extension to the expiry date (specify below including need, justification, stocks held) 5h Renewal of trials permits 5i Change of pack size (within existing range) 5j Commercial withdrawal of an authorised use (specify below including reason, stocks held) 5k Other changes not covered above (include ‘current’ details and ‘proposed’ changes) 3 Form CRD2 Version 04/22 Part C – Extent of authorisation (Note: If you are making a change to an existing product, you cannot change the extent of authorisation using this form. A change to a product using this form can only be GB only to GB only, NI only to NI only or GB&NI to GB&NI.) 6 Where will your application apply 6a Great Britain and Northern Ireland – where conditions of evaluation will be identical 6b Great Britain Only (Scotland, England and Wales) 6c Northern Ireland Only Part D – Product identity 7 Identity of CURRENT product (complete section 8 for a NEW product and to show changed details) 7a Product name (or Code number) 7b MAPP number (if applicable) 7c Authorisation Company holder name Address Company Registration Number 7d Marketing Company company name Address Company Registration Number 7e Current Notice of Authorisation Number(s) (NANUM(s)) 7f Active substance(s) and content (list all using common names) Active g/kg %w/w g/l %w/v 4 Form CRD2 Version 04/22
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