Person for Pharmacovigilance (LRPPV) for coordinating and managing the Regulatory Pharmacovigilance requirements Regulatory Authority requirements relating to Pharmacovigilance and safety for Aspen and Alliance Partner Partner products, including Pharmacovigilance inspections, ensuring that adequate procedures and systems are are in place for the Pharmacovigilance activities to be carried out at Pharmacare in line with global and HOD or Executive in the management of Aspen Pharmacovigilance (PV) Department which acts as affiliate PV
Specialist ensures that all activities related to pharmacovigilance (PV) for both Abbott EPD investigational and that pose a threat locally or globally to pharmacovigilance processes or endanger regulatory compliance implementation of local commercial pharmacovigilance agreements and local pharmacovigilance service agreements - Due
Specialist ensures that all activities related to pharmacovigilance (PV) for both Abbott EPD investigational and that pose a threat locally or globally to pharmacovigilance processes or endanger regulatory compliance implementation of local commercial pharmacovigilance agreements and local pharmacovigilance service agreements Due
report directly to the Head of Medical and Pharmacovigilance. Main Duties and Responsibilities: Provide the pharmacovigilance standard of practice for all company products Ensure the pharmacovigilance team the relevant person in Quality Assurance/ Pharmacovigilance/ Medical Affairs Qualifying Requirements:
with all regulations and maintain comapanys pharmacovigilance requirements. DUTIES AND RESPONSIBILITIES: Follow-up of Adverse Drug Reactions (ADRs), • Pharmacovigilance training of local staff • Answering of requests Maintenance of dossiers and updating thereof o Pharmacovigilance experience / knowledge of collecting and reporting
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
promotional materials. management of local pharmacovigilance activities Quality: Responsible for: quality potential opportunities Management of local Pharmacovigilance activities Quality: Operate at appropriate
appropriate contacts with country Supply Chain, Pharmacovigilance, TS, W&D and Businesses are maintained with internal and external stakeholders: Pharmacovigilance, W&D, Supply Chain, Compliance, Technical
appropriate contacts with country Supply Chain, Pharmacovigilance, TS, W&D and Businesses are maintained with internal and external stakeholders: Pharmacovigilance, W&D, Supply Chain, Compliance, Technical
appropriate contacts with country Supply Chain, Pharmacovigilance, TS, W&D and Businesses are maintained with internal and external stakeholders: Pharmacovigilance, W&D, Supply Chain, Compliance, Technical