This role involves contributing to the monitoring of the tolerability profile of LFB products within the Medicines Safety department. Responsibilities include responding to pharmacovigilance communications, medically assessing data, managing operational cases, drafting various pharmacovigilance documents like protocol sections and signal detection reports, participating in regulatory meetings, and ensuring effective implementation of risk management plans.
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laboratoire biopharmaceutique
Le groupe LFB est un laboratoire biopharmaceutique proposant aux professionnels de santé des médicaments dérivés du plasma ou de protéines recombinantes.