7th Annual European Medical Device Quality Assurance and Regulatory Affairs Conference

The medical device industry thrives by quickly launching products; entering new markets; and adhering to QARA requirements for competitiveness. Mastering diverse regulations is essential; and maintaining high-quality design and materials ensures safety. Robust quality assurance and regulatory affairs policies are crucial for risk identification and timely market entry. The 7th Annual European Medical Device Quality Assurance and Regulatory Affairs Conference by TT Lifesciences will gather top QARA professionals. They will discuss regulatory strategies; quality enhancement; and QARA integration throughout the product lifecycle. Attendees will enjoy live content; interactive sessions; case studies; Q&A sessions; and networking with regulatory bodies; manufacturers; and innovators.