Online workshop: Mastering Medical Requirements Gathering for Successful Product Development

Why Attend Our Lecture Series?

1. Industry-Specific Insights:

Gain a deep understanding of the unique challenges and considerations in the healthcare domain, including patient safety, regulatory compliance, and data privacy.

2. Comprehensive Stakeholder Engagement:

Learn techniques for identifying and prioritizing key stakeholders such as patients, healthcare providers, and regulatory bodies to ensure all critical perspectives are captured.

3. Regulatory and Compliance Mastery:

Navigate complex healthcare regulations like HIPAA, GDPR, and FDA standards with confidence, ensuring your products comply with all necessary legal requirements.

4. Practical Requirements Gathering Techniques:

Master various techniques including interviews, surveys, observations, and workshops to gather precise and actionable requirements directly from your users.

5. Effective Documentation and Management:

Utilize best practices and tools for documenting, managing, and maintaining requirements, ensuring traceability and alignment with project goals.

6. User-Centered Design Principles:

Implement user-centered design methodologies to create intuitive and effective medical products that meet the real needs of end-users.

7. Addressing Challenges and Ensuring Success:

Overcome common challenges such as miscommunication, scope creep, and stakeholder conflicts with proven strategies and best practices.

8. Ethical and Privacy Considerations:

Ensure your products adhere to the highest ethical standards and protect patient privacy throughout the development process.

9. Keeping Up with Emerging Trends:

Stay ahead of the curve with insights into the latest trends and technologies in healthcare, such as AI, IoT, and telemedicine, and their impact on requirements gathering.

10. Hands-On Case Studies and Practical Examples:

 Learn from real-world case studies and practical examples that illustrate successful requirements gathering and product development in the medical field.

Why Choose Us?

Our lecture series is tailored to equip your team with the essential skills and knowledge required for successful medical product development. By attending, you'll ensure your products are user-friendly, compliant, and positioned for success in the competitive healthcare market.
Invest in your team’s expertise and the future success of your medical products. Join us for this invaluable lecture series and transform your approach to medical requirements gathering.
 

About lecturer:

Aljaž Podboršek has extensive knowledge in the field of medical devices, which he has acquired over the past 20 years. His expertise encompasses both the development of medical devices and the legislation that governs them. He has also gained experience in the establishment of various quality management systems. During his time at a medical device manufacturer, Aljaž successfully integrated quality management systems into the company's operations. He also played an active role in the development, production, and compliance of medical devices with regulations and quality management systems in various markets. Currently, Aljaž holds the position of quality manager at a medical device manufacturer. He is also an auditor of quality management systems and technical files for medical devices at SIQ, a Slovenian company that provides certification and training services.

Additional information: Bojan Varga, phone: +386 1 477 81 08, e-mail: bojan.varga@siq.si