The medical device industry is highly regulated, with stringent requirements set by different regulatory bodies such as the FDA. Compliance with regulations is essential for ensuring product safety and efficacy, and quality control is not a one-time effort. It involves continuous improvement methodologies to enhance the quality of products over time.
Scope
- Quality control ensures safety and efficacy of medical devices
- Technological advancements in the medical field can impact regulations
- Medical device regulation is increasingly shaped by a push and pull between global harmonization and regional divergence
Reasons to Buy
- Understand how medical devices are regulated and classified
- Understand how technology is impacting regulations now and in the future
- Learn about the different trends that are impacting how different countries are regulating medical devices
Table of Contents
- Executive Summary
- Players
- Thematic Briefing
- Trends
- Industry Analysis
- Sector Scorecards
- Glossary
- Further Reading
- Thematic Research Methodology
- About the Analyst
- Contact the Publisher
