Executive Development Programme in Medical Affairs and Regulatory Affairs
-- ViewingNowThe Executive Development Programme in Medical Affairs and Regulatory Affairs is a certificate course designed to provide professionals with the essential skills for career advancement in the pharmaceutical industry. This programme emphasizes the importance of compliance, strategy, and communication in medical and regulatory affairs, making it highly relevant for professionals in these fields.
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โข Medical Affairs Overview: Understanding the role, responsibilities, and best practices in medical affairs
โข Regulatory Affairs Overview: An introduction to regulatory affairs, guidelines, and compliance
โข Pharmacovigilance: Monitoring and managing adverse drug reactions and patient safety
โข Clinical Trial Regulation: Navigating regulations, guidelines, and processes for clinical trials
โข Scientific Communication: Developing and delivering effective scientific communications
โข Medical Marketing and Promotion: Compliant marketing and promotion strategies for medical products
โข Stakeholder Management: Building and maintaining relationships with key stakeholders
โข Global Regulatory Landscape: Understanding regional and global variations in regulatory requirements
โข Medical Affairs and Regulatory Affairs Collaboration: Effective collaboration and alignment between medical and regulatory teams
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