The Human Medicines Regulations 2012 No. 1916

PART 3 U.K. [F1 Manufacture and distribution of medicinal products and active substances

Textual Amendments

F1 Pt. 3 heading and Pt. 3 Ch. 1 inserted (20.8.2013) by The Human Medicines (Amendment) Regulations 2013 (S.I. 2013/1855), regs. 1(1), 4

CHAPTER 1 U.K. Interpretation

Interpretation U.K.

A17.   In this Part “manufacture”, in relation to an active substance, includes any process carried out in the course of making the substance and the various processes of dividing up, packaging, and presentation of the active substance.]