Global Certificate in Regulatory Affairs for IVDs
-- ViewingNowThe Global Certificate in Regulatory Affairs for IVDs is a comprehensive course that equips learners with critical skills necessary for navigating the complex regulatory landscape of In Vitro Diagnostic (IVD) devices. With the increasing demand for IVDs in healthcare, there is a growing need for professionals who understand the intricacies of global regulatory requirements.
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⢠Global Regulatory Framework for IVDs
⢠IVD Classification and Categorization
⢠Quality Management System for IVDs
⢠Pre-market Requirements for IVDs
⢠Clinical Evidence and Evaluation for IVDs
⢠Labeling and Packaging Requirements for IVDs
⢠Post-market Surveillance and Vigilance for IVDs
⢠Regulatory Affairs for In Vitro Diagnostic Medical Devices: Challenges and Best Practices
⢠Regulatory Intelligence and Strategy for IVDs
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