Section 31B The Authority's register of serious adverse events and serious adverse reactionsF1
United Kingdom
(1)
The Authority shall keep a register containing information provided to it under this Act about any serious adverse event or serious adverse reaction.
(2)
The Authority shall make such of the information included in the register as it considers appropriate available to the public in such manner as it considers appropriate.
Annotations
Textual amendments
- F1
Ss. 31A, 31B inserted (25.5.2007 for certain purposes, otherwise 5.7.2007) by The Human Fertilisation and Embryology (Quality and Safety) Regulations 2007 (S.I. 2007/1522), regs. 1, 24