• Number: 639/PP/GRO/IMA/17/1133/9952

The results will contribute to a report on the implementation and functioning of the regulations on drug precursors. The Commission must submit this report to the European Parliament and the Council of the European Union by 31 December 2019. 

During the study, the following 5 tasks must be carried out in line with Better Regulation principles:

• Task 1 - Establishing evaluation methodology
• Task 2 - Providing information on the implementation of the regulations, while assessing their effectiveness, efficiency, coherence, relevance and EU added value
• Task 3 - Assessing the need for additional action to monitor and control suspicious transactions with non-scheduled substances
• Task 4 - A stakeholders' consultation and an open public consultation
• Task 5 - A validation workshop

Important

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