The Q-Sub Program gives you pre-submission feedback straight from the FDA. It’s a simple way to streamline submission. If you have a medical device in development, take a look at how Avania can support you throughout the process. It Takes Avania. Read the White Paper.
Research Report: The Costly Impact of Ineffective Requirements Management
This report conducted by Axendia, a leading Life-Sciences Analyst firm, walks through groundbreaking research about the costly impact of ineffective requirements management in the medical device industry, including: The impact of ineffective closed-loop requirements management process. The importance of requirements to achieve better outcomes. The negative impact on budgets, traceability, V&V activities when relying on […]