Paivi Turta

Director - Quality & Regulatory Compliance Medbase Oy

Päivi Turta is Director of Quality and Regulatory Compliance at Medbase, with over 20 years of experience in quality and regulatory affairs within in vitro diagnostics and medical devices. Her career has increasingly focused on medical device software, and she currently works exclusively with software-based medical device products. She leads Medbase’s regulatory strategy and QMS and oversees quality and regulatory compliance across the software product lifecycle, from design and development to conformity assessment and post-market activities. Her expertise includes MDR, ISO 13485, IEC 62304, and ISO 14971. She is passionate about enabling innovation through effective regulatory compliance.

Seminars

Thursday 10th December 2026
MedTech Match-Up Roundtable Discussions: Benchmarking Success & Opportunities Across Every Stage of Growth
12:00 pm

Whether you’re building your first software-enabled device or scaling AI and cybersecurity programmes across a global portfolio, organisations face very different challenges depending on their size and maturity. Join peers from similarly sized companies for an interactive roundtable discussion designed to share experiences, benchmark approaches and uncover practical solutions to common software development, AI and compliance challenges.

Start-Up Sprint for Small & Emerging Innovators

  • How to build quality and regulatory foundations with limited resources while accelerating growth
  • Discussing challenges and questions around balancing agility versus compliance
  • Lessons learned from training teams about adequate compliance and optimising processes to empower efficiency

Scaling for Success for Mid-Sized Medical Device Manufacturers

  • Strategies for scaling software teams, AI initiatives and compliance processes without sacrificing agility

Enterprise Exchange for Large Medical Device Manufacturers

  • Managing global software portfolios, AI governance, cybersecurity programmes and complex regulatory requirements across multiple product lines
  • The Small-Team Paradox: Development, QA, Regulatory, Systems, UX, Cybersecurity, Program Management, etc. all need to have a voice in product development. How small can teams realistically be?
Paivi Turta - 4th Medical Device Software Development Europe