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4 – 5 April 2017
Helsinki, Finland
Website: http://europa.eu/
30 March 2017
Brussels, Belgium
Website: http://europa.eu/
22 March 2017
Brussels, Belgium
Website: http://www.europarl.europa.eu/
20 – 22 March 2017
Brussels, Belgium
Website: http://europa.eu/
20 March 2017
Brussels, Belgium
Source: http://europa.eu/
28 – 30 June 2017
Belgrade, Serbia
Website: http://www.chem.bg.ac.rs/eurovariety/
25 – 29 June 2017
Barcelona, Spain
Website: http://www.bienal2017.com/
19 – 22 June 2017
Ponta Delgada, Portugal
Website: http://www.spe2017.com/
18 – 22 June 2017
Brescia, Italy
Website: http://www.corbellasummerschool.unimi.it/
18 – 22 June 2017
Oslo, Norway
Website: http://icce2017.org/
12 – 14 June 2017
Nynäshamn, Sweden
Website: http://www.oorgan.se/
10 May 2017
Brussels, Belgium
Website: http://www.euchems.eu
19 – 22 April 2017
Poreč, Croatia
Website: http://www.euchems.eu/
5 April 2017
Valletta, Malta
Website: http://www.euchems.eu/
Deadline: 9 May 2017
Website: https://ec.europa.eu/
Deadline: 2 May 2017
Website: https://eacea.ec.europa.eu/
Deadline: 20 April 2017
Website: http://ec.europa.eu/
Deadline: 20 April 2017
Website: http://ec.europa.eu/
Deadline: 20 April 2017
Website: http://ec.europa.eu/
Deadline: 20 April 2017
Website: http://ec.europa.eu/
Deadline: 7 April 2017
Website: http://ec.europa.eu/
This impact assessment will look into how to optimise the internal market’s industrial property legal framework relating to supplementary protection certificates (SPC) and patent research exemptions (particularly, Bolar exemptions) for sectors whose products are subject to regulated market authorisations. SPCs are an intellectual property right that constitute an extension (of up to five years) to the term of a patent right (of twenty years). They aim to offset the loss of effective patent protection that occurs due to the compulsory and lengthy testing and clinical trials that products require prior to obtaining regulatory marketing approval. The Bolar patent exemption aims at speeding up the entry of generic medicines into the market by allowing early preparatory development on generics to obtain pre-market regulatory approval even when the SPC of the reference medicine is still in force. The Commission will conduct an evaluation and impact assessment of all relevant provisions and options for modernising the SPC Regulations and the provisions of the Directives dealing with the Bolar exemption.
Website: http://ec.europa.eu/
The European Food and Safety Authority (EFSA) is currently running a survey on the topic of uncertainty, to improve the way that EFSA communicates and explains the scientific uncertainties related to its assessments. Even when there is strong evidence that something will happen, there will almost always be some uncertainty about the outcome, a point that should always be taken into consideration when taking decisions or making assessments. The survey should take about 10 minutes, and the participants are welcome to provide additional advice the topic.
Source: http://www.efsa.europa.eu/
The consultation aims to gather comments and perspectives from various stakeholders and the general public on the relevance of the Erasmus+ programme’s objectives, the effectiveness of the measures taken to achieve them and the efficiency of their implementation. It will also gather views on the coherence of the programme and its added value in relation to the challenges and opportunities in education, training, youth and sport sectors, compared to what could be achieved by Member States only. The consultation also covers the Erasmus+ predecessor’s programmes (e.g. Lifelong Learning, Youth in Action, Erasmus Mundus, etc.) and contain> s forward looking questions regarding a possible successor programme to Erasmus+ in 2020.
Deadline: 31 May 2017
Website: http://ec.europa.eu/