\n\t\t\t\t\t\t\t \t\t\tPURPOSE : to present the intiative of the Kingdom of Sweden witha view to the adoption of a Council Decision establishing a system of special forensic profiling analysis of synthetic drugs. \nCONTENT : this proposal aims to establish a European system of laboratories with the aim of carrying out special forensic profiling analysis on samples of seized synthetic drugs for the purpose of the prevention, detection, investigation and prosecution of criminal offences. The laboratories that are to carry out special analyses on samples of synthetic drugs are designated in the Annex of this proposal.\nThe designated laboratories shall have two main tasks in particular:\n- to perform a special analysis of synthetic drugs of the samples transmitted to them on the behalf of the Member States;\n- to determine whether the samples analysed matches with other samples analysed by that laboratory.\nFurthermore, the designated laboratories shall apply the best possible chemical processes for the special analysis and shall keep a record of all samples analysed in order to allow checking to be made whether match exists between samples. These laboratories shall, for the work carried out on the basis of this decision, be funded by the Member States in whose territory they are located.\nAs far as the Member States are concerned, they have an important role to play in the seizing of the synthetic drugs at production sites and thereafter transmitting these samples to the designated laboratories for special analysis.\nLastly, in accordance with Article 4(4) of the Europol Convention, criminal intelligance or investigative data related to a seizure that is to be transmitted for special analysis shall be transmitted to Europol at the same time as the transmission of the sample itself to a designated laboratory. The designated laboratories shall keep a record of all special analyses carried out for a period of at least five years. �
\n\t\t \t\t\t\t\t\t
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\n\t\t\t\t\t\t\t \t\t\tIn a general statement which makes a point highlighting the progress made on the subject of the knowledge of the effects of Ketamine and its dangers, the Council encourages EMCDDA and Europol to continue monitoring, in the framework of their respective work programmes and in cooperation with the Member States, the manufacture, trafficking, patterns of use and health consequences of ketamine, particularly the trends in recreational use.\nIt suggests that possible improvements in the control of diversion be discussed with the chemical and pharmaceutical industry, bearing in mind the importance of ensuring the continued availability of ketamine for medical and veterinary use. It also encourages Member States to present proposals for research on the effects of ketamine use to be considered under the Fifth Framework Program for Research and Development.\nLastly, the Council invites the Commission to take into account the outcome of the risk assessment of ketamine in the evaluation of the effectiveness of the Joint Action called for in the EU Action Plan on Drugs 2000-2004.�
\n\t\t \t\t\t\t\t\t
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\n\t\t\t\t\t\t\t \t\t\tThe committee adopted the report by Charlotte CEDERSCHIÖLD (EPP-ED, S) broadly approving the Swedish initiative under the consultation procedure, subject to a number of amendments, most of which were aimed at streamlining and clarifying the text. However, the committee also made a few substantive changes, which included removing the possibility of using transport by courier for the transmission of samples. It argued that such a means of transport did not provide the security guarantees that such sensitive products required. Provision should also be made for keeping the authorised means of transport under constant review and agreeing on alternative secure means of transport where necessary. The committee also wanted the Decision to be subject to evaluation at least two and no more than four years after its entry into force, thereby leaving enough time to assess its effectiveness while not allowing too long a period to go by before taking any necessary corrective measures. For practical reasons (i.e. the long time it could take for any criminal offences to be prosecuted), it also wanted the period during which the sample transmission forms were archived to be extended from five to ten years. �
\n\t\t \t\t\t\t\t\t
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\n\t\t\t\t\t\t\t \t\t\tThe European Parliament endorsed the report by Mrs Charlotte CEDERSCHIÖLD (EPP/ED, S) on the Swedish initiative with a view to the adoption of a Council Decision establishing a system of special forensic profiling analysis of synthetic drugs. (Please refer to the previous document).�
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\n\t\t\t\t\t\t\t \t\t\tPURPOSE : to present the intiative of the Kingdom of Sweden witha view to the adoption of a Council Decision establishing a system of special forensic profiling analysis of synthetic drugs. \nCONTENT : this proposal aims to establish a European system of laboratories with the aim of carrying out special forensic profiling analysis on samples of seized synthetic drugs for the purpose of the prevention, detection, investigation and prosecution of criminal offences. The laboratories that are to carry out special analyses on samples of synthetic drugs are designated in the Annex of this proposal.\nThe designated laboratories shall have two main tasks in particular:\n- to perform a special analysis of synthetic drugs of the samples transmitted to them on the behalf of the Member States;\n- to determine whether the samples analysed matches with other samples analysed by that laboratory.\nFurthermore, the designated laboratories shall apply the best possible chemical processes for the special analysis and shall keep a record of all samples analysed in order to allow checking to be made whether match exists between samples. These laboratories shall, for the work carried out on the basis of this decision, be funded by the Member States in whose territory they are located.\nAs far as the Member States are concerned, they have an important role to play in the seizing of the synthetic drugs at production sites and thereafter transmitting these samples to the designated laboratories for special analysis.\nLastly, in accordance with Article 4(4) of the Europol Convention, criminal intelligance or investigative data related to a seizure that is to be transmitted for special analysis shall be transmitted to Europol at the same time as the transmission of the sample itself to a designated laboratory. The designated laboratories shall keep a record of all special analyses carried out for a period of at least five years. �
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\n\t\t\t\t\t\t\t \t\t\tIn a general statement which makes a point highlighting the progress made on the subject of the knowledge of the effects of Ketamine and its dangers, the Council encourages EMCDDA and Europol to continue monitoring, in the framework of their respective work programmes and in cooperation with the Member States, the manufacture, trafficking, patterns of use and health consequences of ketamine, particularly the trends in recreational use.\nIt suggests that possible improvements in the control of diversion be discussed with the chemical and pharmaceutical industry, bearing in mind the importance of ensuring the continued availability of ketamine for medical and veterinary use. It also encourages Member States to present proposals for research on the effects of ketamine use to be considered under the Fifth Framework Program for Research and Development.\nLastly, the Council invites the Commission to take into account the outcome of the risk assessment of ketamine in the evaluation of the effectiveness of the Joint Action called for in the EU Action Plan on Drugs 2000-2004.�
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\n\t\t \t\t\t\t\t\t
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\n\t\t\t\t\t\t\t \t\t\tThe European Parliament endorsed the report by Mrs Charlotte CEDERSCHIÖLD (EPP/ED, S) on the Swedish initiative with a view to the adoption of a Council Decision establishing a system of special forensic profiling analysis of synthetic drugs. (Please refer to the previous document).�
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