About

Timothy Bubb has more than 10 years’ experience in quality assurance and regulatory affairs roles, with breadth and depth of knowledge across regulatory, engineering, clinical, design and development, and quality assurance disciplines. He has a passion for empowering innovation in medical devices and brings insight and pragmatism to projects bringing complex lifesaving and life-enhancing products to market.

Contributions

EXPERT VIEW

NAVIGATING THE AI REVOLUTION IN THE MEDICAL DEVICES SECTOR: BETWEEN INNOVATION AND REGULATION

Timothy Bubb discusses the potential impact of artificial intelligence and machine learning on the healthcare and drug delivery industries, with an overview of the differing regulatory approaches taken by the EU, US FDA and UK MHRA towards this novel area of digital health.

More contributions

EXPERT VIEW

ENSURING PATIENT SAFETY AMIDST MEDICAL DEVICE REGULATION DELAYS WITH PMS

Timothy Bubb discusses the five steps to setting up an effective post-market surveillance process.