Whitepaper

Drug accountability is a need of the hour to ensure regulatory compliance during clinical trials. IRT tends to be of utmost help at this time ensuring patient safety and helping you in earning approval. This whitepaper highlights some key areas of compliance that can be ensured along with drug accountability with the help of IRT.

Along with this, there are a few other things that this paper covers such as:

• Challenges in managing paper-based drug accountability
• How does IRT help?
• The future prospects