Executive Development Programme in Drug Safety Risk Management
-- ViewingNowThe Executive Development Programme in Drug Safety Risk Management is a certificate course designed to empower professionals with the necessary skills to excel in the pharmaceutical industry. This programme emphasizes the importance of risk management in drug development and post-marketing surveillance, addressing critical issues that impact patient safety and organizational success.
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โข Introduction to Drug Safety Risk Management: Understanding the importance of drug safety risk management, its role in public health, and the key stakeholders involved.
โข Pharmacovigilance: The science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problem.
โข Risk Management Planning: Developing a comprehensive plan for monitoring, assessing, and minimizing potential risks associated with drug products.
โข Signal Detection and Evaluation: Identifying and evaluating potential safety concerns using epidemiological, clinical, and statistical methods.
โข Risk Communication: Effectively communicating risk information to healthcare providers, patients, and regulatory authorities.
โข Benefit-Risk Assessment: Evaluating the benefits and risks of drug products to inform decision-making and regulatory actions.
โข Pharmacoepidemiology: The study of the use and effects of drugs in large populations.
โข Regulatory Affairs and Compliance: Understanding the regulatory landscape and ensuring compliance with drug safety risk management requirements.
โข Quality Management in Drug Safety: Implementing and maintaining quality systems to ensure the accuracy and reliability of drug safety data.
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