Case processing times

For cases with fixed application deadlines, the recommended case processing time commences upon expiry of the application deadline.
The processing times given below indicate the maximum timeframe within which most cases will be processed. In cases where the Danish Environmental Protection Agency is unable to meet the target case processing time, the private individual/company/authority will be informed of this and given an indication of the anticipated date for completion of processing.
All cases will of course be processed as quickly as possible. This means that many cases will be processed before the end of the specified processing time.
The Danish Environmental Protection Agency’s various types of administrative cases are not comparable. Consequently, the target times for processing vary from one type of case to another.

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<tbody>
<tr>
<th>
Authorisation of biocides in accordance with the Biocidal Products Directive (the active substance is included in Annex I)
</th>
<th>
Target
</th>
</tr>
<tr>
<td>
Verification of completeness of an application for authorisation
</td>
<td>
3 months
</td>
</tr>
<tr>
<td>
Authorisation of a biocidal product (both new and already marketed in DK)
</td>
<td>
12 months
</td>
</tr>
<tr>
<td>
Verification of completeness of an application for mutual recognition
</td>
<td>
15 days
</td>
</tr>
<tr>
<td>
Mutual recognition
</td>
<td>
120 days
</td>
</tr>
<tr>
<td>
Mutual recognition of a low-risk product
</td>
<td>
60 days
</td>
</tr>
<tr>
<td>
Registration of a low-risk product
</td>
<td>
60 days
</td>
</tr>
<tr>
<td>
Authorisation of a product within a frame-formulation
</td>
<td>
60 days
</td>
</tr>
</tbody>
</table>

<table border="0" style="width: 65%; margin-left: auto; margin-right: auto;">
<tbody>
<tr>
<th>
Authorisation of biocides in accordance with existing national regulations under the transitional arrangements
</th>
<th>
Target
</th>
</tr>
<tr>
<td>
Application for authorisation of products containing active substances which are new to Denmark
</td>
<td>
1½-2 years
</td>
</tr>
<tr>
<td>
Renewal of an authorisation
</td>
<td>
1 year
</td>
</tr>
<tr>
<td>
Application for authorisation of new products containing active substances which have already been approved ("me-too products")
</td>
<td>
Up to 1½ years, depending on complexity and the need for external consultation
</td>
</tr>
<tr>
<td>
Application for extended use, changes to formulation
</td>
<td>
Up to 1½ years, depending on complexity and the need for external consultation
</td>
</tr>
<tr>
<td>
Authorisation of parallel products
</td>
<td>
3-6 months
</td>
</tr>
<tr>
<td>
Private testing
</td>
<td>
3 months
</td>
</tr>
</tbody>
</table>

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