DIA MedTech Conclave 2025 will cover key areas shaping the future of medical devices, in vitro diagnostics, combination products, and Software as a Medical Device (SaMD). The sessions will provide expert insights, regulatory updates, and best practices across the MedTech ecosystem.

• Regulatory Pathways for Market Authorization – India & global requirements for medical devices and diagnostics.
• Quality & Risk Management – Design validation vs. verification, conformity assessment, and compliance strategies.
• Fundamentals and emerging Regulatory perspective in AI and Software as Medical device – Decoding the EU vs US requirements. 
• Why are emerging cybersecurity trends and updates in medical devices so important [Software as Medical Device & AI in MedTech]?
• Regulatory & Clinical Considerations for SaMD – Standards, compliance, and evaluation of Software as a Medical Device.
• Clinical Evaluation & Evidence Generation – Strategies for regulatory submissions and market access.
• Risk Management for Medical Devices – Implementation of ISO 14971 and best practices.
• Safety & Post-Market Surveillance – Materiovigilance, complaint management, and post-marketing clinical follow-up.
• Challenges and Opportunities for Indian Medtech Companies while going global

This conclave provides a comprehensive learning experience, addressing critical aspects of MedTech innovation, regulation, and patient safety.

DIA MedTech Conclave 2025 is designed for professionals involved in the development, testing, regulation, and commercialization of medical devices, in vitro diagnostics, combination products, and Software as a Medical Device (SaMD). 
 

• R&D and Product Development Teams – Understand the latest trends in MedTech innovation and regulatory expectations.
• Regulatory Affairs and Quality Assurance Professionals – Who wish to implement actionable items and updates
• Regulatory Affairs & Compliance Professionals – Stay updated on evolving global and Indian regulatory requirements.
• Clinical Research & Medical Affairs Professionals – Gain insights into clinical evaluation, post-market surveillance, and materiovigilance.
• Healthcare & Policy Experts – Engage in discussions on safety, compliance, and market access.
• Start-ups & Entrepreneurs – Connect with industry leaders and explore pathways to global markets
  

DIA MedTech Conclave 2025 is designed to provide participants with in-depth knowledge and practical insights into the evolving MedTech landscape. By attending, participants will:

• Understand Global & Indian Regulatory Pathways: Navigate marketing authorization and compliance for medical devices, IVDs, and combination products.
• Master Quality System & Risk Management: Learn best practices for design validation, verification, and conformity assessment.
• Explore AI & SaMD Regulations: Gain insights into compliance, standards, and evaluation of Software as a Medical Device in EU and US.
• Strengthen Clinical & Post-Market Strategies: Enhance knowledge of clinical evaluation, post-marketing surveillance, and materiovigilance.
• Network & Collaborate: Connect with regulators, industry leaders, start-ups, and academia to drive MedTech innovation.

This conclave is a must-attend for professionals in regulatory affairs, quality, clinical research, and MedTech development aiming for global excellence.