[Guidance]Responding to COVID-19: Making the Pivot to Medical Device Production
In response to the global COVID-19 pandemic, companies around the world are looking to adapt their manufacturing capabilities to support the manufacture and distribution of in-demand medical devices such as ventilators and face masks. Despite the urgent need for these supplies, however, companies must still meet stringent medical devices industry requirements.
What’s in This Guidance?
This guidance explores the regulatory challenges companies face when pivoting their operations to support the global response to COVID-19, and how they can be met by leveraging third-party support and expertise.
Key Insights Include:
- Pandemic-related exemptions and due diligence issues impacting the medical technology sector.
- The role of supply chain data management in meeting a variety of regulatory obligations.
- An overview of the steps and tasks required to broadly comply with the sector’s exacting requirements.
- …And more!
Download your copy of the guidance now!