GLOSSARY ENTRY (DERIVED FROM QUESTION BELOW) | ||||||
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18:59 Jan 24, 2021 |
Russian to English translations [PRO] Medical - Medical: Pharmaceuticals / Материалы регистрационного досье по качеству лекарственных средств | |||||||
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| Selected response from: Peter Shortall United Kingdom | ||||||
Grading comment
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Summary of answers provided | ||||
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3 +3 | high-technology medicinal products |
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4 | advanced therapy medicinal products (ATMPs) |
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high-technology medicinal products Explanation: Council of the European Communities Directive 93/41/EEC of 14 June 1993 repealed Directive 87/22/EEC on the approximation of national measures relating to the marketing of high-technology medicinal products, as this directive had been superseded by Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products (5) and by Council Directive 88/182/EEC of 22 March 1988 amending Directive 83/189/EEC laying down a procedure for the provision of information in the field of technical standards and regulations (6). https://en.wikipedia.org/wiki/Directive_93/41/EEC |
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