EU GDP definition

EU GDP means the European Union Good Distribution Practices. “EU GMP” means the European Union Good Manufacturing Practices.
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EU GDP means European Union good distribution practice; "EU-GMP" means European Union good manufacturing practice; "Eurasia Infused" means Eurasia Infused Cosmetics Inc.; "EuroLife" means EuroLife Brands Inc.;
Sample 1

Examples of EU GDP in a sentence

  • The contraction in EU GDP is expected to be far deeper than during the financial crisis in 2009 and adverse social effects will be inevitable.

  • The volume of aid approved in 2009 was EUR 82.5 billion (0.7% of EU GDP).

  • With 1.8% of EU GDP, down from 2.2% in 2009, infrastructure investment activities in the Union in 2016 were about 20% below investment rates before the global financial crisis.

  • VAT raised slightly more than EUR 1 trillion in 2015, which corresponds to 7% of EU GDP or 17.6% of total national tax revenues1.

  • The contraction in EU GDP in 2020 is expected to be around 7.5%, far deeper than during the financial crisis in 2009.

  • Put differently, the pharmaceutical market accounted for close to 2% of annual EU GDP.

  • Therefore, the pharmaceutical market accounted for close to 2% of annual EU GDP.

  • Investment rates in 2016 represented 1.8% of EU GDP, down from 2.2% in 200910.

  • The completion of on-going FTA negotiations could potentially boost EU GDP by 2% (EUR 250 billion).

  • Enhancing competitiveness could lead to an additional total economic gain of about 2.6% of the EU GDP.

Related to EU GDP

  • EU GDPR means Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC.

  • GDPR means the General Data Protection Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • MFDA means the Mutual Fund Dealers Association of Canada;

  • Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following: