MEDICAL AFFAIRS

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Our Medical & Regulatory affairs team are up to date with the latest pharmaceutical and healthcare practices to ensure consistency with the most recent guidelines, regulations and clinical publications. 

•  Conduct disease and product trainings for internal and external stakeholders. 
•  Promotional material review and approval, and medical writing.  
•  Project Management for medical programs.  
•  Lead and conduct continuous medical education (CME’s) programme.  
•  Identifying key opinion leaders and stakeholder mapping. 
•  Creation of medical/scientific slide decks.  
•  SOP Writing.