Nada Ahmed Mohamed

Pharmacovigilance SpecialistFull Time

• Job Details:· Maintain the pharmacovigilance system and its quality. · Archiving of pharmacovigilance data and documents. · Preparation, revision, and responsible for submission of all pharmacovigilance documents (PBRER, RMP, ACO, DHPC, questionnaires...) to the Pharmaceutical Vigilance General Administration (PVGA) within the specified time frames. · collaborate with the QPPV in preparing the PSMF. · Routine literature search to follow any updates Concerning BioMed products and report it to PVGA. · Committed to PVGA meetings along with QPPV and responding to all PVGA 's requests including the provision of correcting or completing information. · Maintain Safety data exchange agreement. · Deliver PV training to all white and blue collar. · Follow up, validation & assessment of ICSRs and notify PVGA in writing using MedDRA coding within the specified time frame.

Pharmacovigilance SpecialistFull Time

• Job Details:· Maintain the pharmacovigilance system and its quality. · Archiving of pharmacovigilance data and documents. · Preparation, revision, and responsible for submission of all pharmacovigilance documents (PBRER, RMP, ACO, DHPC, questionnaires...) to the Pharmaceutical Vigilance General Administration (PVGA) within the specified time frames. · collaborate with the QPPV in preparing the PSMF. · Routine literature search to follow any updates Concerning P&C products and report it to PVGA. · Committed to PVGA meetings along with QPPV and responding to all PVGA 's requests including the provision of correcting or completing information. · Maintain safety data exchange agreement. · Deliver PV training to all white and blue collar. · Follow up, validation & assessment of ICSRs and notify PVGA in writing using MedDRA coding within the specified time frame.

Deputy QPPVFull Time

• Job Details:· Maintain the pharmacovigilance system and its quality. · Archiving of pharmacovigilance data and documents. · Preparation, revision, and responsible for submission of all pharmacovigilance documents (PBRER, RMP, ACO, DHPC, questionnaires...) to the Pharmaceutical Vigilance General Administration (PVGA) within the specified time frames. · collaborate with the QPPV in preparing the PSMF. · Routine literature search to follow any updates Concerning P&C products and report it to PVGA. · Committed to PVGA meetings along with QPPV and responding to all PVGA 's requests including the provision of correcting or completing information. · Maintain safety data exchange agreement. · Deliver PV training to all white and blue collar. · Follow up, validation & assessment of ICSRs and notify PVGA in writing using MedDRA coding within the specified time frame.