Paragraph 14D F1
The licence holder must maintain an MM master file for each MM medicinal product specified in the licence.
Annotations
Textual amendments
- F1
Sch. 4 Pts. 1A, 1B inserted (23.7.2025) by The Human Medicines (Amendment) (Modular Manufacture and Point of Care) Regulations 2025 (S.I. 2025/87), regs. 1(2), 35