Use (Amendment) Regulations, 2022
Statutory Text (3 Articles)
L.N. 283 of 2022
MEDICINES ACT
(CAP. 458)
Manufacture and Importation of Medicinal Products for Human
Use (Amendment) Regulations, 2022
IN EXERCISE of the powers conferred by article 106 of the
Medicines Act, the Minister responsible for public health, after
consultation with the Licensing Authority, has made the following
regulations:-
The title of these regulations is the Manufacture and
Importation of Medicinal Products for Human Use (Amendment)
Regulations, 2022 and these regulations shall be read and construed as
one with the Manufacture and Importation of Medicinal Products for
Human Use Regulations, hereinafter referred to as "the principal
regulations".
In regulation 11A of the principal regulations, the words
"31st December 2022" shall be substituted by the words "31st December
2024".
€0.09