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(2014; 2 pages)
Based on the official process for developing monographs for inclusion in The International Pharmacopoeia (Ph.Int.) as outlined in World Health Organization (WHO) Technical Report Series, No. 970 (Annex 1), the following process was elaborated to fit the specific purpose of development and update of radiopharmaceutical specifications, a joint project between the International Atomic Energy Agency (IAEA) and WHO, in close collaboration with the Council of Europe (CoE) and other parties prepared to join.