1. Ordinary legislative procedure or co decision? The European decision making process is extremely complicated and often it takes several years before a legislative proposal becomes European law. The EU decision making procedure comes about as a result of decisions taken by the institutional triangle, made up of
  • the Council (representing national governments),
  • the European Parliament (representing the people) and
  • the European Commission (a body independent of EU governments that upholds the collective European interest).

The EU’s standard decision making procedure was known as co decision. However, after the entry into force of the Lisbon Treaty on 1 December 2009, the Treaty on the Functioning of the European Union (TFEU) has become one of the principle legal sources of the primary law of the EU and it uses the term ‘ordinary legislative procedure’ (since it become the most common procedure for the majority of EU legislations). However, it is not incorrect to use the term ‘co decision’ to describe the procedure in the common language.

An overview of the procedure is available as follows

  • Explanatory note on the ordinary legislative procedure / co decision
  • VIDEO How does the ordinary legislative procedure work?
  1. The Tobacco Products Directive (TPD) case study

Europe pays a hefty price for its slow action on tobacco, both in economic costs and harm to its citizens’ health and wellbeing. Tobacco is a major risk factor of cancer, 1 cardio vascular disease 2 and other chronic diseases such as the Chronic Obstructive Pulmonary Disease (COPD) 3

The Tobacco Products Directive (2001/37/EC) regulates the manufacture, presentation and sale of tobacco products in the EU 28 Member States. This covers the use of health warnings on packs, the prohibition of descriptions such as ‘mild’ or ‘light’, the maximum tar, nicotine and carbon monoxide yields, and the prohibition of the sale of tobacco for oral use.

In February 2012, the Commission proposal was ready to go to impact assessment which has been finished in August 2012. The inter service consultation started immediately, but additional review by the legal services through an explicit demand from the Commission Secretary General blocked the process. The resignation of Commissioner Dalli on 16th of October 2012 postponed the progress of the Directive even further.

During his hearing by the European Parliament, the Commissioner candidate, Tonio Borg, committed to prioritise the dossier once appointed. Officially nominated on 28th of November 2012, Commissioner Borg launched the inter service consultation as soon as he was in post and promised to have the Commission proposal by the end of 2012. On 19th of December 2012, the European Commission proposal was released.

Ordinary Legislative Provedure and the TPD The TPD is subject to ordinary legislative procedure which is still in the first reading procedure, as follows

  1. The Commission submitted its proposal for the TPD to both the Council and the European Parliament on 20 December 2012
  1. The Council adopted its General Approach on 21 June 2013.
  1. The European Parliament, adopted by 560 votes to 92, with 32 abstentions, amendments to the proposal on its plenary session on 8 October 2013 and referred the file back to the main responsible ENVI committee which entered into negotiations with the Council in order to reach an agreement in the first reading.

Trilogue negotiations on the TPD In order for the two co legislators to come to an agreement, the so called trilogue negotitations commenced in October 2013 between the Council, the European Parliament and the Commission. Four rounds of negotiations were held on (23 October, 12 November, 2 December and 16 December).

During the final trilogue meeting on 16 December, the negotiating parties came to a preliminary agreement which needed the approval of the Member States. On 18 December 2013, Members States approved this compromise during the meeting of the Permanent Representatives of Member States (COREPER) during the first reading procedure and it will not reach second reading. In practice, the TPD now remains to be approved by the European Parliament during plenary vote in order to come into effect. This is due to occur once translation of the text is completed and expected in March or April 2014.

Further information about technical details

  • Overview on the revision of the TPD
  • Calendar of the main steps of the TPD negotiations
  • Calendar on the TPD trilogue negotiations
  • European Legislative Observatory summarizing some key legislative steps
  • VIDEO How it works? Trilogue
  1. Questions & Answers about e cigarettes

Nicotine Containing Products (NCPs) or electronic cigarettes?

Nicotine containing products (NCP) is the wider category, it contains different products (ex. patches, gum etc.) containing nicotine, including e cigarettes. The e cigarette is the narrower category which is (according to the latest proposal ‘a product, or any components thereof including cartridges and the device without cartridge, that can be used for consumption of nicotine containing vapour via a mouth piece’)

Are e cigarettes tobacco products?

We have to make a clear distinction between the logical and the legal way of assessment. Under the current EU legal framework, e cigarettes are not considered as tobacco products since they do not contain pure tobacco as conventional cigarettes do. The assumption that nicotine as a substance was derived from tobacco does not mean automatically that e cigarettes can be regarded as tobacco products.

However, the legal definition can be different. Regulating e cigarettes similarly to tobacco products is just a method of codification. If the co legislators find it appropriate, they can include e cigarettes under the Tobacco Products Directive (TPD). In that case, e cigarettes are treated as tobacco products and the specific legal rules laid down in the TPD apply to them.

Are the current e cigarette EU market harmonised?

No. The legal fact that the General Product Safety Directive (GPSD) is applicable to them (among other EU rules) does not mean that there is an EU wide regulatory harmonisation of e cigarettes. The situation is the opposite since the GPSD is a complementary legal act, Member States are allowed to adopt more specific rules. That is why there are divergent regulations in different member states and some of them regulate e cigarettes as human medicines (see the Annexes of the EPHA Briefing Regulation of Nicotine Containing Products (NCPs) including electronic cigarettes)

What is the relevance of different national court decisions about single e cigarette products?

There are several national legal cases where the national courts confirmed that a single e cigarette product cannot be considered, as a human medicines (ex. in Germany or in Estonia). However, due to lack of EU level harmonisation, national courts can come to a different condusion, as well a French court
recently ruled that electronic cigarettes qualify as tobacco products and as such can only be sold by licensed tobacconists under French law, threatening to put specialist e cigarette sellers across the country out of business.

What are the implications of such decisions?

As a result of lack of European harmonisation, national courts interpret the existing national law on e cigarettes and the legal interpretation of national courts have limited legal impacts the selected decisions only affect the specific product which is subject to the given procedure. Moreover, most European states follow the Roman law based legal system which means that case law does not settle the internal legal system and courts interpret legislation made by the national legislators.

An example of a court decision in the Netherlands The Dutch court considered that a given e cigarette product could not be classified as medicines in the Netherlands. The Dutch national authorities classified the e cigarette subject to the legal proceeding as pharmaceutical products but the court overruled this decision. The judgment explains that the examined e cigarettes cannot be considered as medicines either by presentation or by function. It says that the pharmaceutical effects on human beings are not strong enough since other products such as wine, coffee, conventional cigarette have similar effects. The court added that the examined e cigarettes were not dangerous enough so they could not be classified based on public health arguments. The Court finished to say that such a regulation could be an obstacle for the internal market. However, it is important to note that this decision concerns only the examined product in the Netherlands which was subject to the legal proceeding. The court stated that there is no unified European position on e cigarettes which would have changed the outcome of the decision.

See the list of similar cases on the ECITA website

Flavours of e cigarettes Some flavours are necessary to make e cigarettes palatable. However there are concerns amongst the public health community regarding the appealing impact of flavours for children / young people.

What is an e cigarette? Does one size fit all?

There are different types of e cigarettes. The presentation of Dr Lynne Dawkins from the e cigarette summit describes e cigarettes and the different types and goes into how effective they are.

  1. Disposables (cigalikes)
  1. Rechargeables with sealed units often similar to disposables or variants on the same product e.g. Vuse make a disposable and for smokers who carry on using longer term a rechargeable which looks almost identical.
  1. Third generation cartomisers which are modular enabling the smoker to adapt them to their own needs as the refill is not sealed but can be adapted and which do not look at all like cigarettes.

Must read documents, should you have further questions

EPHA Guide The EU and Health This guide is designed to equip the reader with two strong skills the ability to understand the role of the EU in shaping public health across the continent and the capacity to identify the various areas in which Brussels works to advance everyone’s well being.

EPHA Briefing Regulation of Nicotine Containing Products (NCPs) including electronic cigarettes The future legislation of nicotine containing products (NCPs) including e cigarettes is part of the ongoing discussion on the revision of Tobacco Products Directive (TPD). In light of the available regulatory options EPHA has identified and presented in a briefing document, EPHA recommends principles of future EU wide NCP legislation, public health requirements of NCPs, and policy recommendations for regulating NCPs.

EPHA related articles

  • Joint press statement Mixed victory for tobacco control in European Parliament’s vote
  • Final countdown public health community calls on European Parliament to vote for a strong Tobacco Products Directive
  • Joint Open Letter to President of European Parliament Philip Morris lobbying activities on the Tobacco Products Directive
  • EPHA Calls for Strong Tobacco Products Directive (TPD) without further delay
  • Sign the ERS petition for a strong Tobacco Products Directive!
  • Global Initiative Don’t Touch the Spanish Tobacco Law
  • EPHA Open Letter to Spanish Prime Minister Smoking should be banned at “Eurovegas”
  • EPHA and Public Health NGOs call for an updated EU Tobacco Products Directive
  • EPHA position paper Revision of the Tobacco Products Directive

Menthol cigarettes face eu ban

Variety of marlboro cigarettes – benson hedges fresh facebook, prince price in spain

The European commission has called for strongly flavoured cigarettes to be banned and unveiled draft legislation to impose graphic images of the risks of smoking on all cigarette packaging.

Reporting that 700,000 people die in Europe every year from smoking related diseases, the costs of treatment for which run to 25bn ( 20bn) plus another 8bn in lost productivity, the commission outlined a battery of measures aimed at curbing smoking.

“We’re not prohibiting smoking we’re making it less attractive for everyone,” said Tonio Borg of Malta, the health commissioner. “Sometimes you need shocking pictures to shock people into stopping smoking.”

The draft directive unveiled on Wednesday has to be endorsed by member governments and the European parliament, which could take three years.

The directive would ban cigarettes with a “characterising flavour”, such as menthol, strawberry or vanilla, on the grounds that they encourage young people to start smoking. “If it’s tobacco, it should look like tobacco and taste like tobacco,” said Borg.

Mandatory pictorial health warnings would cover at least 75% of cigarette packets.

Borg said the commission was not treating people “in a stupid way” or waging a crusade against smoking. “Everyone will benefit,” he said.

Glenis Wilmott, Labour leader in the European parliament, said “Cigarette packets should look like they contain a dangerous drug, rather than perfume or lipstick. The commission proposal does not go far enough. We need to get rid of all branding from cigarette packets, as it is the only space that the tobacco industry has left to market their products.

“Tobacco is still the leading cause of preventable death across the UK, Europe and the world. One in two long term smokers are killed by tobacco, and the smoking rate amongst young women is on the rise.”

The tobacco directive has been wreathed in controversy since October, when Borg’s predecessor as health commissioner, John Dalli, also from Malta, was sacked by the commission president, Jose Manuel Barroso, over allegations of sleaze. The claims involved Swedish tobacco lobbyists who were said to be seeking the lifting of an EU ban on snus, a type of orally administered, smoke free tobacco.

Dalli has denied wrongdoing. Under the proposals, snus remains outlawed in the EU except, as previously, in Sweden.

The measures directed at cigarette smoking were not extended to cigars and pipe tobacco, on the grounds that their consumption was insufficiently widespread and remained unattractive to young people.

The commission said 70% of smokers start before the age of 18, and the aim of the draft law was to cut cigarette smoking by 2% within five years.

“This proposal ensures that attractive packaging and flavourings are not used as a marketing strategy,” said Borg.