At study completion, all the supply needs to be returned, accounted and destructed. It is recommended to ensure these services are conducted in a timely manner throughout study duration.
- Returns from study sites
Returns are received and stored in a designated separated area while providing relevant documentation
- Accountability of returns
The customer and drug characteristics defines the accountability level to be performed, either per kit level or per inner kit components
- Destruction of returns and supply extra amounts
Upon Sponsor's approval the supply is sent for destruction