This training program on clinical investigation of medical devices is designed for Quality professionals in the Pharma sector. It addresses the challenge of ensuring compliant clinical investigations that meet regulatory expectations for safety, performance, and data integrity. Participants will gain the ability to establish quality oversight, evaluate investigation documentation, and maintain compliance with ISO 14155 requirements. The program uses clinical investigation scenarios, compliance reviews, and documentation evaluation exercises to ensure practical application.
Course Content
Fundamentals of Medical Device Clinical Investigations
5 Topics
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ISO 14155 Requirements for Clinical Investigation Quality
5 Topics
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Quality Oversight in Clinical Study Planning
5 Topics
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Documentation Control and Data Integrity
5 Topics
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Monitoring and Compliance Management
5 Topics
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Clinical Investigation Reporting and Regulatory Support
5 Topics
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Inspection Readiness and Compliance Assessment
5 Topics
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Meet Your Instructor
Deep-domain, High Precision L&D - delivered directly by Renowned Industry Practitioners HUKSA
159 Course
13 Student
Offered by Huksa, this L&D program is led by elite industry veterans—CXOs and Functional Heads with 25+ years of deep-domain expertise. You have the flexibility to customize the curriculum, select your preferred expert, and align the program to your organization’s specific objectives. Connect with the Huksa team to explore our array of top-tier trainers available for this course!
₹80,000.00
This course includes:
- Lessons 7
- Topics 35
- Duration 1 Day
- Quizzes 0
- Language English
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