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Explore a wide range of free and certified Medical devices online courses. Find the best Medical devices training programs and enhance your skills today!
Explore how Software Design Documents bridge requirements and implementation in medical software, covering regulatory standards, architecture definition, and user interface design for safety.
Master the essential Software Design Document template for medical software, covering architecture, workflows, UI design, dependencies, and risk management strategies.
Explore System Requirement Specification for medical software, focusing on neurosurgery applications, risk analysis, and translating user needs into functional specifications.
Master the essential components of System Requirement Specification templates for medical software, from functional requirements to regulatory compliance and testable documentation.
Discover how to identify true user needs in medical software by distinguishing engineer vs. customer perspectives, conducting effective meetings, and considering all stakeholders.
Explore the complete medical software development process from user needs identification through design, verification, validation, deployment, and retirement phases.
Explore medical software life cycles and IEC 62304 standard, covering risk classifications, development models, and quality management systems for compliant projects.
Discover cybersecurity fundamentals for medical software developers, covering patient safety, data integrity, authentication, encryption, NIST framework, and FDA risk classifications.
Explore regulatory pathways for medical software approval across US, EU, and China, covering risk classifications, FDA processes, and key compliance requirements.
Explore the FDA's evolution from food regulation to medical software oversight, examining landmark incidents like Therac-25 and core principles of efficacy, safety, and security.
Explore medical software fundamentals, regulatory processes, and development lifecycle in this Yale introduction to digital health opportunities.
Explore regulatory classifications, risk management, and lifecycle essentials for safe medical software development through real-world neurosurgery case studies.
Explore software testing fundamentals for medical applications, covering methodologies from unit to system testing, white/black box approaches, and quality assurance strategies.
Explore FDA's General Principles of Software Validation (GPSV) guidance, covering hardware vs software validation differences and essential compliance requirements.
Master fundraising strategies for medical software startups, from seed rounds to VC, including pitch techniques, risk mitigation, and alternative funding sources.
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