Harmonizing Global Regulatory Strategies to Simplify Medical Device Submissions & Expand Market Reach
Time: 9:00 am
day: Pre-Conf Track B Morning
Details:
- Navigating complex regulatory landscapes across key global markets by discussing advanced strategies for interpreting and applying the regulatory requirements and submission processes for the FDA, EU, Japan, and other regions
- Harmonizing global submissions by gaining insights into streamlining regulatory submissions across multiple regions, minimizing redundancy, and optimizing time-to-market
- Managing cross-jurisdictional challenges by exploring common hurdles in managing multi-market regulatory approvals, including varying requirements for clinical trials, risk management, and post-market surveillance, and discovering strategies to overcome these challenges effectively
