CLINICAL SAFETY
Ensures that Novartis complies with the strict legal reporting requirements
for pharmacovigilance by processing all adverse events according to
local/global SOPs
Clinical Safety Monitors Key Task:
Processing all adverse events reported from clinical trials
and those occurring for marketed products ensuring company complies
with Central Clinical Safety SOPs.
Provision of value added safety information from global databases
to support key internal customers.
Evaluating and prioritising cases for reportability to health
authority ensuring the company complies with Key Performance Indicator
(KPI) measures for adverse event reporting as laid out in Central
SOPs and Irish Medicines Board.
Reporting and follow up of all Irish spontaneous adverse events
reports ensuring compliance with quality KPI and that optimal
outputs attained for health authority and Central Clinical Safety.
Training sales representatives and other personnel involved
in handling adverse events.
Care Guide
Nails speak volumes. Consider the perfectly sculpted fingernails of the society lady compared with lack-lustre, chipped and grubby nails. Nails speak, not only of social status, but may also reflect health or lack of it.
