To account all the Supplies of Clinical Trial is a Regulatory requirement. Traditionally people used to use paper based or Excel based tracking of the Supplies. This is tedious, time consuming and…
The regulation brings digital enablement to the forefront, compelling electronic instructions for use.
EU MDR is turning digitization on its head. This new regulation, which goes into effect Ma…
20%
of risks are addressed by teams in clinical projects.
30%
of the risks or either siloed or trapped in functions.
50%
A vast majority (50%) are unreported and lost.
If you kno…
Unfortunately, most sponsors and CROs use multiple applications to manage their clinical studies. Integrating multiple applications may be challenging for example reporting through multiple ap…
Clinical trials are more complex than ever and a robust, reliable & cost efficient clinical supply strategy is vital more than ever before. The number and complexity of issues affecting supply…
