Chwilio Deddfwriaeth

The Human Medicines (Amendment) (Modular Manufacture and Point of Care) Regulations 2025

 Help about what version

Pa Fersiwn

  • Y Diweddaraf sydd Ar Gael (Diwygiedig)
  • Gwreiddiol (a wnaed Fel)
 Help about opening options

Dewisiadau AgorExpand opening options

Status:

Dyma’r fersiwn wreiddiol (fel y’i gwnaed yn wreiddiol). Dim ond ar ei ffurf wreiddiol y mae’r eitem hon o ddeddfwriaeth ar gael ar hyn o bryd.

Insertion of new regulations 17A and 17B (manufacturing of MM and POC medicinal products)

This adran has no associated Memorandwm Esboniadol

6.  After regulation 17 (manufacturing of medicinal products) insert—

Manufacturing of MM medicinal products

17A.  A person may not manufacture or assemble an MM medicinal product unless—

(a)it is specified in a manufacturer’s licence (MM); and

(b)there is an MM master file relating to that product and it is manufactured or assembled in accordance with that master file.

Manufacturing of POC medicinal products

17B.  A person may not manufacture or assemble a POC medicinal product unless—

(a)it is specified in a manufacturer’s licence (POC); and

(b)there is a POC master file relating to that product and it is manufactured or assembled in accordance with that master file..

Yn ôl i’r brig

Options/Cymorth