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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โข Global Regulatory Framework for IVDs
โข IVD Classification and Categorization
โข Quality Management System for IVDs
โข Pre-market Requirements for IVDs
โข Clinical Evidence and Evaluation for IVDs
โข Labeling and Packaging Requirements for IVDs
โข Post-market Surveillance and Vigilance for IVDs
โข Regulatory Affairs for In Vitro Diagnostic Medical Devices: Challenges and Best Practices
โข Regulatory Intelligence and Strategy for IVDs
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- BasicUnderstandingSubject
- ProficiencyEnglish
- ComputerInternetAccess
- BasicComputerSkills
- DedicationCompleteCourse
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- NotAccreditedRecognized
- NotRegulatedAuthorized
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- ThreeFourHoursPerWeek
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- TwoThreeHoursPerWeek
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