Be Prepared... It Could Happen
Download this white paper to get your recall procedures in place.
Medical device recalls are a fact of life and competitors love to find out that you’ve had one. Regardless of recall classification (Class I, II, or III), a recall procedure is instrumental in working in concert with a company’s post-market surveillance and agreements with suppliers. Companies should not assume there is never going to be an issue with a product and not have these procedures in place up front.
In this white paper you will learn how to:
- Conduct a post-market risk analysis and document the conclusion
- Form a safety review board within your company comprised of a cross-functional team
- Ensure recall procedures are in place and that you follow the same process every time, regardless of recall classification.
- Have traceability to all devices up front
- And much more!