Masterclass Certificate in Regulatory Affairs for IVDs

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The Masterclass Certificate in Regulatory Affairs for IVDs is a comprehensive course that provides learners with critical skills in the regulatory affairs sector, specifically for In Vitro Diagnostic (IVD) devices. This course is essential for professionals seeking to navigate the complex regulatory landscape and ensure compliance with IVD regulations.

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AboutThisCourse

With the increasing demand for IVD devices and the growing emphasis on patient safety, there is a high industry need for experts with a deep understanding of regulatory affairs. This course equips learners with the skills to manage regulatory compliance, liaise with regulatory agencies, and ensure the safe and effective use of IVD devices. By completing this course, learners will gain a competitive edge in their careers, with the ability to drive regulatory strategy, manage regulatory risks, and ensure compliance with regulatory requirements. The Masterclass Certificate in Regulatory Affairs for IVDs is an essential course for professionals seeking to advance their careers in the regulatory affairs sector.

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CourseDetails

• Introduction to Regulatory Affairs for IVDs: Understanding the regulatory landscape, key players, and regulations for In Vitro Diagnostic devices (IVDs)
• Classification of IVDs: Learning the risk-based classification system for IVDs and its impact on regulatory requirements
• Quality Management System (QMS): Implementing a QMS in compliance with ISO 13485 and FDA Quality System Regulation
• Clinical Evidence and Performance Evaluation: Generating and reporting clinical data to demonstrate the safety and performance of IVDs
• Labeling and Instructions for Use (IFU): Designing and reviewing labeling and instructions for proper use of IVDs
• Pre-market Notification (510(k)) and Approval (PMA): Navigating the FDA's pre-market review process for IVDs
• European Union (EU) Regulations for IVDs: Compliance with EU IVD Regulation (EU) 2017/746 and In Vitro Diagnostic Medical Device Regulation (IVDR)
• Post-market Surveillance and Vigilance: Implementing strategies for monitoring, reporting, and analyzing post-market data for IVDs
• Global Harmonization and International Regulations: Staying updated on global regulatory trends and international standards for IVDs

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  • BasicUnderstandingSubject
  • ProficiencyEnglish
  • ComputerInternetAccess
  • BasicComputerSkills
  • DedicationCompleteCourse

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  • NotAccreditedRecognized
  • NotRegulatedAuthorized
  • ComplementaryFormalQualifications

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FastTrack GBP £149
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AcceleratedLearningPath
  • ThreeFourHoursPerWeek
  • EarlyCertificateDelivery
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StandardMode GBP £99
CompleteInTwoMonths
FlexibleLearningPace
  • TwoThreeHoursPerWeek
  • RegularCertificateDelivery
  • OpenEnrollmentStartAnytime
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  • DigitalCertificate
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MASTERCLASS CERTIFICATE IN REGULATORY AFFAIRS FOR IVDS
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UK School of Management (UKSM)
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05 May 2025
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