Professional Certificate in Ethical Drug Development Practices
-- viewing nowThe Professional Certificate in Ethical Drug Development Practices is a comprehensive course designed to empower learners with the essential skills required in the pharmaceutical industry. This program emphasizes the importance of ethical practices in drug development, a critical aspect in creating safe and effective medications.
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Course Details
Here are the essential units for a Professional Certificate in Ethical Drug Development Practices:
• Introduction to Ethical Drug Development Practices: Understanding the ethical principles, guidelines, and regulations that govern drug development.
• Good Clinical Practice (GCP): Learning the international ethical and scientific quality standard for designing, conducting, recording, and reporting trials involving human subjects.
• Data Integrity in Drug Development: Ensuring the accuracy, completeness, and reliability of data generated during drug development.
• Informed Consent: Understanding the process of obtaining informed consent from patients or participants involved in clinical trials.
• Pharmacovigilance: Learning the methods and processes for monitoring, detecting, assessing, and preventing adverse drug reactions.
• Ethical Considerations in Clinical Trial Design: Exploring the ethical implications of trial design, including inclusion/exclusion criteria, randomization, and blinding.
• Ethical Issues in Drug Marketing and Promotion: Understanding the ethical considerations surrounding drug marketing, promotion, and advertising.
• Conflict of Interest in Drug Development: Learning how to identify, manage, and disclose conflicts of interest that may arise during drug development.
• Ethical Considerations in Drug Pricing and Access: Exploring the ethical implications of drug pricing, affordability, and access.
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