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ISSN 2041366130 NOVEMBER 2009MHRA updates its serious
breaches guidanceEMEA moves towards
pharmacovigilance
transparency Medicines and Healthcare products Regulatory Agency
(MARA) has updated its
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What is mhra updates its serious?
The MHRA updates its serious adverse events reporting system.
Who is required to file mhra updates its serious?
Manufacturers, healthcare professionals, and marketing authorization holders are required to file MHRA updates its serious adverse events.
How to fill out mhra updates its serious?
To fill out MHRA updates its serious adverse events, specific forms and documentation are required to be completed and submitted to the MHRA.
What is the purpose of mhra updates its serious?
The purpose of MHRA updates its serious adverse events is to monitor and assess the safety of medicines and medical devices in the UK.
What information must be reported on mhra updates its serious?
Information such as details of the adverse event, patient information, medicinal product information, and any action taken must be reported on MHRA updates its serious adverse events.
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