The Human Medicines Regulations 2012

Periodic safety update reports

This section has no associated Explanatory Memorandum

10.  The reference to “the EMA” in regulations 191(1) (obligation on holder to submit periodic safety update reports: general requirements) and 192(3) (obligation on holder to submit periodic safety update reports: derogation from general requirements) should be read on both occasions as a reference to “the relevant competent authorities”.