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Paragraph 2 Introductory

Changes not yet applied. Later legislation changes this provision in ways not yet written into the text below:

The requirements of this Schedule supplement those of Council Directive 92/27/EEC relating to:

(a)

special warnings necessary for particular medicinal products;

(b)

the legal status for supply to the patient, in accordance with Council Directive 92/26/EEC;

(c)

identification and authenticity.