Artificial Intelligence and Machine Learning in Medical Technology
Fundamentals and Emerging Regulations

An FDAnews FREE Webinar • Sponsored by ComplianceQuest
Thursday, March 18, 2021 · 11:00 a.m. – 12:00 p.m. EDT

Are you ready for the revolution in medical technology?

Artificial intelligence (AI) and machine learning (ML) will be among the top innovations this decade, especially when it comes to medical science, medical devices, in-vitro diagnostics, clinical evaluation, healthcare in general and even in quality systems software.

Don’t be left behind by the AI and ML revolution that is propelling devicemakers to redesign technology and change processes in unprecedented ways. This free webinar explains what you must know about the fundamentals and emerging regulations.

While the possibilities are vast, AI and ML are accompanied by many issues and challenges for manufacturers, clinicians, technicians, engineers, quality assurance, regulatory affairs, clinical professionals and regulators.

Sundeep Agarwal, General Manager of Compliance & Regulatory Affairs for Datt Mediproducts Ltd., will explain the basics and emerging regulations coming out of today’s — and tomorrow’s — regulatory environment. He’ll address manufacturers’ challenges in designing a compliant AI framework that is safe, effective and beneficial for human health around the world.

Webinar Takeaways:

  • Introduction to artificial intelligence (AI)
  • Overview of the regulatory framework of AI in the U.S. and EU
  • AI-based software classification
  • Quality system and good machine learning practices (GMLP)
  • Medical specialties where current AI applications are used
  • Challenges and issues with AI
  • Potential benefits of AI in medical devices, healthcare and pharmaceuticals

Get a handle on AI and ML with this free webinar. Don’t miss the medical technology revolution. Join us by registering today.

Who Will Benefit

  • Product Design Engineers
  • IT Professionals
  • Quality Assurance and Regulatory Affairs Professionals
  • Regulatory Consultants
  • Clinical Experts
Sign Up for FREE Below

Meet Your Presenter

Sundeep Agarwal

General Manager of Compliance & Regulatory Affairs
Datt Mediproducts Ltd.

Sundeep Agarwal is the General Manager of Compliance & Regulatory Affairs for Datt Mediproducts Ltd., India. He is a globally sought-after leader, speaker and consultant with a decade of experience in the field of quality assurance and regulatory affairs, quality management systems (QMS), product design and development, commercial, scale-up, industrial manufacturing and clinical studies of medical devices. Mr. Agarwal frequently joins medical device industry- and government-collaborated conferences as a speaker and panelist on ISO 13485, EU Medical Device Regulation (EU-MDR), U.S. FDA, ISO 14971, medical device single audit program (MDSAP), combination devices and more.