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    Thairis sin, tá táirgí sonracha ann, amhail radachógais a úsáidtear mar tháirgí íocshláinte imscrúdaithe diagnóiseacha, ar míchuí na rialacha ginearálta maidir le lipéadú a fheidhmiú ina leith i bhfianaise na gcoinníollacha an-rialaithe atá ann d'úsáid radachógas i dtrialacha cliniciúla.

    Moreover, there are specific products, such as radiopharmaceuticals used as diagnostic investigational medicinal product, where the general rules on labelling are inappropriate in view of the very controlled setting of the use of radiopharmaceuticals in clinical trials.

    Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC Text with EEA relevance