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a.
a)
Last Update: 2017-04-06
Usage Frequency: 67
Quality:
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b.
Last Update: 2017-04-06
Usage Frequency: 2
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(a)
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Last Update: 2017-04-06
Usage Frequency: 1
Quality:
dan is- sommarju ie a ornat l- a
this summary was last updated in 08-2007.
Last Update: 2011-10-23
Usage Frequency: 2
Quality:
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barra minn hekk, g andu ji i ppre entat rmp a ornat • meta ti i r evuta informazzjoni dida li jista ’ jkollha impatt fuq l- ispe ifikazzjoni tas- sigurtà attwali, fuq il- pjan tal- farmakovi ilanza jew fuq l- attivitajiet li jnaqqsu r- riskji • fi mien 60 jum minn meta tintla aq mira importanti (farmakovi ilanza jew tnaqqis tar- riskji) • fuq talba ta ’ l- emea
in addition, an updated rmp should be submitted • when new information is received that may impact on the current safety specification, pharmacovigilance plan or risk minimisation activities • within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached • at the request of the emea
Last Update: 2011-10-23
Usage Frequency: 1
Quality:
Warning: This alignment may be wrong.
Please delete it you feel so.
