EU-GMP definition

EU-GMP means European Union Good Manufacturing Practices (“EU-GMP”) standards.
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EU-GMP means the good manufacturing practices established by European Union regulations.
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EU-GMP means good manufacturing practice, being the standard required under the Laws of the European Union.
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Examples of EU-GMP in a sentence

  • SUPPLIER develops documents (protocols, reports, etc.) in accordance with AMWHV and EU-GMP guidelines for all performed activities.

  • The Company has also secured supply from an EU-GMP certified facility to meet demand in Germany and sell products under the IMC brand.

  • Medical cannabis sold under the Purchase Commitment will be fulfilled primarily from the Company's EU-GMP certified supply partner in Europe.

  • In Europe, IMC has established a medical cannabis operation, first with its distribution subsidiary in Germany and augmented by strategic agreements with certified EU-GMP Standard suppliers, making it one of very few medical cannabis companies with fully integrated operations in Europe.

  • In order to strengthen its strategic position, IMC purchased an EU-GMP certified narcotics distributor, Adjupharm, which has an experienced management team in place.

  • Besides this, Orchid’s facilities are approved worldwide, including approvals like EUGMP, PMDA-Japan, and ANVISA-Brazil.

  • Adjupharm, an EU-GMP certified subsidiary of the Company, has entered into a twelve-month sales agreement with a medical cannabis distributor in Germany.

  • In Europe, IMC has established a medical cannabis operation first with its distribution subsidiary in Germany and augmented by strategic agreements with certified EU-GMP Standard suppliers, making it one of the only medical cannabis companies with fully integrated operations in Europe.

  • In doing so, the TMIG Agreement provided IDP Canada with the exclusive right to export all of the Medicinal Plants and/or Medicinal Plant Derivatives grown, processed and/or purchased by TMIG in the DRC for processing into Cannabinoid Oil at IDP Canada- contracted EU-GMP certified Medicinal Plant Derivative extraction, processing, and packaging facilities around the world for subsequent sale throughout IDP Canada’s international buying network.

  • Arrange GMP shipping service through an EU-GMP compliant logistics service provider.


More Definitions of EU-GMP

EU-GMP means European Union Good Manufacturing Practices (“EU-GMP”) standards. “FDA” means the U.S. Food and Drug Administration.
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Related to EU-GMP

  • 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.

  • EU SCCs means the annex found in the European Commission decision of 4 June 2021 on standard contractual clauses for the transfer of personal data to third countries pursuant to Regulation (EU) 2016/679 of the European Parliament and of the Council (available as of August 1, 2021 at ▇▇▇▇.▇▇▇▇▇▇.▇▇/▇▇▇/dec_impl/2021/914/oj) and any amendments, replacements, or updated standard contractual clauses as recognized and approved by the European Commission from time to time.

  • GMP means the amount proposed by Contractor and accepted by Owner as the maximum cost to Owner for construction of the Project in accordance with this Agreement. The GMP includes Contractor’s Construction Phase Fee, the General Conditions Cost, the Cost of the Work, and Contractor’s Contingency amount.

  • 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;

  • CFDA means the Code of Federal Domestic Assistance assigned to a federal grant.