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European Community Directives

Council of European Communities, Directive 89/107/EEC, December 21, 1988, on the approximation of the laws of the Member States concerning food additives authorised for use in foodstuffs intended for human consumption, 1988. [Pg.582]

Decreasing levels in sludge has been reported in several European countries since nineties16 17 18. But we can expect the growing amounts of sludge production after introducing the European Community Directive (COM 91/271) on wastewater treatment, requires the installation of treatment systems in all towns with over 2000 inhabitants before 2005. The need to monitor PCDD/Fs loads from this source remains. [Pg.212]

Protection of water sources is critical to economic viability as well as to human and environmental health. This has been evident for many decades, but just in the 1980s, the European Community started to adopt legislative measures to evaluate and preserve groundwater and also to implement bans on pesticides which at first concerned mainly persistent organochlorine compounds. Along the years, various European Community Directives have addressed these issues in the European Union, among them ... [Pg.378]

LC techniques are widely diffused for the determination of hydrophilic but not volatile and thermally unstable pesticides. Since the European Community Directive [68] indicates 0.1 pg L" as the concentration threshold level for a single pesticide in waters destined for human consumption, to quantify these concentration levels, suitable pre-concentration and extraction procedures must be generally performed prior to the HPLC determination. The extraction methods are based on LLE, MAE, on-line continuous flow liquid membrane extraction (CFLME), and mainly on SPE and SPME. Many SPE procedures are used the packing materials are graphitized carbon, ODS, styrene-divinylbenzene co-polymers, or selective phases based on immunoafflnity. The extraction can be performed on- and off-line, manually, or in a semi-automated way. [Pg.540]

European Community, Directive of the Council Meeting of 21 December. Offic. J. Eur. Community, 40 27(1988). [Pg.489]

The competitive electrochemical immunosensing strategy can easily reach the required LOD for potable water orange juice (MRL 0.1 pgL ) established by the European Community directives with very simple sample pretreatments. The orange juice samples spiked with atrazine was first diluted five times with PBST pH 7.5 buffer and then filtered through 0.22 pm filter before measurement. The features of these approaches are described in detail in the following section. [Pg.482]

The competitive electrochemical immunosensing strategy can easily reach the required LOD for potable water orange juice (MRL 0.1 pgL-1) established by the European Community directives with very simple sample pretreatments. [Pg.488]

Table 4.7. Abbreviated list of authorized feed enzymes in the European Community (Directive 70/524/EEC and Annex to Directive 82/471/EEC). Table 4.7. Abbreviated list of authorized feed enzymes in the European Community (Directive 70/524/EEC and Annex to Directive 82/471/EEC).
European Communities, Directive 67/548/EEC Annex V Part B. http //ecb.jrc.it/testing-methods/... [Pg.130]

European Community Directive 91/356/EEC (Principles and guidelines of good manufacturing practice for medicinal products for human use) Annex 11. [Pg.618]

In Europe, regulatory exclusivity is more complex. More specifically, the countries may choose between a 10 year or 6 year period. According to European Community Directive 87/21, the national states can protect pharmaceutical products for 6 or 10 years from first marketing approval in the European Community. An exception to this is biotech products for which a 10 year period applies for all European countries. The countries that have chosen 10 or 6 years are presented in Table 3. [Pg.2614]

Municipal supplies whilst often arising from one or several of the sources listed above are frequently pretreated by the Regional Water Authority in order to meet the requirements for potable quality laid down by The European Community directives given in Table 8.2. [Pg.180]

In the United Kingdom, regulation is derived from the Medicines Act of 1968, which provides a comprehensive system of licensing affecting most aspects of the sale of medicinal products. It also contains provisions on related matters, such as pharmacovigilance and the requirements for the reporting of adverse events (AEs). The Medicines Act encompasses measures contained in European Community Directives, including the first on the control of medicines, introduced in 1965. The Medicines Act led to the creation of various... [Pg.598]

As well as domestic legislation, there is extensive European legislation governing member states. The European Community has over the years established measures to harmonize the regulation of medicines throughout Europe. In 2001, all European Community Directives adopted between 1965 and 1999 on the regulation of medicines were consolidated into a Community Code . At the time, the Code could not incorporate the new Clinical Trials Directive harmonizing EU controls on the approval and conduct of clinical trials (i.e. Directive 2001/20/EC). The Community Code has, however, since been amended to take into account the Directive s ethics. [Pg.599]

The UK joined the European Community in 1973, but the data requirements for granting marketing authorisations have, since the implementation of the Medicines Act 1968, been in accordance with European Community Directive 65/65/EEC and the subsequent Directive 75/318/EEC as amended, which elaborated on the requirements for... [Pg.599]

An European Community Directive on the disposal of PCBs, with its requirements for the preparation of inventories, labehng of all significant PCB holdings, and the tighter regulation of PCB treatment facihties, is committed to phasing out identifiable PCBs by 2010. [Pg.674]

European Community Directive 65/65/EEC Now codified into Community Code 2001/83/EC. [Pg.420]

Other new regulations (Display Screen Equipment, Work Equipment, Personal Protective Equipment) implement aspects of the MHSW 1992 and Workplace Regulations in more detail. These also fulfil some of the European legislation that has shaped our practice since 1993. This relates to the European Community Directives issued by the Council of Ministers under Article 118A of the Treaty of Rome. [Pg.13]

In terms of safety, a computer system appears ostensibly to pose little risk to the user and its presence in a classroom seems to offer little risk to pupils. Reputable companies produce machines that comply with electrical safety regulations. Except for portables, computers are usually static in nse, being placed on a desk or a trolley, and thus may appear to be relatively safe. However, experience of working with ICT has shown me that there are significant safety issues of which every teacher should be aware. These same issues have been used to frame the legal context that surrounds the use of ICT in the workplace via the European Community Directive (EEC) on the use of Visual Display Units (VDUs) (EEC, 1990). The potential hazards are compounded when there are multiple computer systems in one room, for example, in a computer lab. The issues that affect pupils, teachers and other school employees who come into contact with ICT are ... [Pg.74]

Commission of the European Communities Directive of the European Parliament and of the Council. Brussels, Belgium 1999. Available at http//europa.eu.int/eur-lex/en/com/pdf/1999/en 599PC0577.pdf. Accessed August 8, 2003. [Pg.554]

The Council of the European Communities, Directive 93/42/EEC, Medical Device Directive (MDD), June 1993. [Pg.614]

Among the various definitions of food additives that can be found in international legislation and accords is the one adopted by the European Union (EU) in its European Community Directive 89/107/EEC of the Council of 21 December 1988 any substance not normally consumed as a food in itself and not normally used as a characteristic ingredient of food whether or not it has nutritive value, the intentional addition of which to food for a technological purpose in the manufacture, processing, preparation. [Pg.1458]

Table 2 European Community Directives (updated on December 2003) ... Table 2 European Community Directives (updated on December 2003) ...
European legislation is compiled in European Community Directives that are published in the Bulletin of the EU. European Community Directives affect the entire EU, setting a time limit for their integration in the legislation of each Member State, after which they are required to be enforced in the entire EU. Table 2 is a catalog of European Community Directives, updated in December 2003, that regulate positive lists of additives, standards for the purity of additives, and the maximum amounts of additives that can be added to different categories of foods. [Pg.1463]


See other pages where European Community Directives is mentioned: [Pg.510]    [Pg.483]    [Pg.124]    [Pg.474]    [Pg.319]    [Pg.488]    [Pg.779]    [Pg.1488]    [Pg.371]    [Pg.121]    [Pg.33]    [Pg.77]    [Pg.600]    [Pg.155]    [Pg.416]    [Pg.417]    [Pg.420]    [Pg.420]    [Pg.116]    [Pg.1461]    [Pg.1462]   
See also in sourсe #XX -- [ Pg.80 , Pg.510 ]




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