Translation of "Concurrent Drug Use Review " (English → French) :

Social Solidarity Revised Directive on transfers of undertakings Social partners’ consultation on cross-border collective bargaining Simplify legislation on information and consultation of workers Follow up of Green Paper on the evolution of labour law European Strategy on Information and Communication Technologies to promote social inclusion and independent living in an ageing society Justice and Home Affairs Follow-up to Green Papers on succession and wills, matrimonial property regimes and the attachment of bank accounts Green Paper and a Policy Plan on the establishment of the second phase of the Common European Asylum System Green Paper on the effective enforcement of judicial decisions Minimum standards relating to the gathering and h ...[+++]andling of evidence with a view to mutual admissibility Communication on drugs policy and on mechanisms to detect, monitor and respond to emerging trends in drug use and drug markets Communication on a more harmonized interpretation of key provisions of the Data Protection Directive Sustainable Management and Use of Resources and Environment Protection Revision of the EU Emission Trading Scheme and a proposal on Carbon Capture and Geological Storage New initiative on Green Public Procurement as part of the Action Plan on sustainable production and consumption New structures for development and demonstration of clean coal technologies Establishment of the new EU Chemicals Agency in Helsinki and implementing legislation on the new chemicals regulation (REACH) Review of the Habitats and Birds Directives, to adapt them to new scientific knowledge Conclusion of the Green Paper’s consultation on a future maritime policy and presentation of an Action Plan |

Perhaps a committee of the House, like the special committee on the non-medical use of drugs, could review the subject matter more comprehensively.

(b) The new narcotic drug or the new synthetic drug is a ‘medicinal product under review’, which is either a medicinal product intended for human use that is under examination in order to be granted a marketing authorisation in one or more Member States or in the European Union in accordance with the provisions of Title III of Directive 2001/83/EC, or a veterinary medicinal product that is under examination in order to be granted a marketing authorisation in one or more Member States or in the European Union in accordance with the pro ...[+++]visions of Title III of Directive 2001/82/EC; or,

4. Calls on the Council and the EU Member States to begin a process of revising the UN Conventions on the occasion of the conference for the mid-term review of UN drug policies to be held in Vienna in April 2003, with the aim of repealing or amending the 1961 and 1971 Conventions with a view to reclassifying substances and legalise the use of drugs for purposes other than medical or scientific ones, and to repealing the 1988 Convention.

I think that Parliament would have seriously failed in its most basic political responsibilities if it had not undertaken a thorough review of the Monitoring Centre’s duties and tabled a set of proposals that represents a thorough overhaul of its operations. We believe that the Drugs Monitoring Centre is crucial, much needed and has a useful role to play in the future of the European Union, but not by means of this report, with whi ...[+++]ch, in essence, the Commission apparently agrees.

In view of the increasing concerns regarding accidents involving the use of medicines and illicit drugs, and in order to review the situation on such a complex issue, the High Level Group on Road Safety decided, at the end of 1997, to reactivate the Working Group on Alcohol, Drugs and Medicines and Driving.