Global Certificate in Health Product Licensing
-- ViewingNowThe Global Certificate in Health Product Licensing course is a comprehensive program designed to meet the growing industry demand for professionals with a deep understanding of health product regulation. This course emphasizes the importance of licensing in the health product industry, covering pharmaceuticals, biologics, and medical devices.
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GBP £ 149
GBP £ 215
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โข Global Regulations in Health Product Licensing: An overview of international regulations and guidelines governing the licensing of health products, including pharmaceuticals, medical devices, and biologics.
โข Clinical Trials and Data Requirements: Discussing the design, conduct, and reporting of clinical trials, as well as the data requirements necessary to support health product licensing applications.
โข Quality Management Systems: An examination of quality management systems and their role in ensuring the consistent quality, safety, and efficacy of health products throughout the product lifecycle.
โข Labeling and Packaging: Exploring the regulatory requirements for labeling and packaging of health products, including the use of appropriate language, symbols, and graphics.
โข Pharmacovigilance and Risk Management: Examining the systems and processes for monitoring, identifying, and managing risks associated with health products, including adverse event reporting and signal detection.
โข Marketing Authorization Applications: A detailed review of the process for submitting marketing authorization applications to regulatory agencies, including the preparation, content, and format of the application.
โข Regulatory Inspections and Audits: Exploring the regulatory inspection and audit process, including preparing for and managing inspections, responding to observations, and addressing findings.
โข Post-Marketing Surveillance and Lifecycle Management: Examining the regulatory requirements for post-marketing surveillance and lifecycle management of health products, including changes to the product, labeling, and manufacturing processes.
โข International Trade and Import/Export Regulations: An overview of the regulations governing the international trade and import/export of health products, including tariffs, customs, and labeling requirements.
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