with all regulations and maintain comapanys pharmacovigilance requirements.
DUTIES AND
of Adverse Drug Reactions (ADRs),
• Pharmacovigilance training of local staff
• Answering of
Maintenance of dossiers and updating thereof
o Pharmacovigilance experience / knowledge of collecting and reporting
the relevant person in Quality Assurance/ Pharmacovigilance/ Medical Affairs Qualification: CA(SA) Experience:
the relevant person in Quality Assurance/ Pharmacovigilance/ Medical Affairs Qualifying Requirements are:
the relevant person in Quality Assurance/ Pharmacovigilance/ Medical Affairs CA(SA) Minimum 8 years relevant
the relevant person in quality assurance/ pharmacovigilance/ medical affairs Core Competencies: Sound
the relevant person in quality assurance/ pharmacovigilance/ medical affairs Core Competencies: Sound
the relevant person in Quality Assurance/ Pharmacovigilance/ Medical Affairs CA(SA) Minimum 8 years relevant
the relevant person in quality assurance/ pharmacovigilance/ medical affairs Third party manufacturers/packers/FPRC:
the relevant person in quality assurance/ pharmacovigilance/ medical affairs Third party manufacturers/packers/FPRC:
reporting and management of drug safety and pharmacovigilance activities in compliance with local and global