Clinical Supplies Technology and IRT Standardization
Every study is special, but when it comes to building an IRT system do we really need to re-invent the wheel every time we pick up a new study protocol? How much can we learn from the teams that came before us, and the work they did in developing standard functionlity?
In this webinar we will examine the 80/20 rule, specifically focusing on ;
- What functionality really needs to be study-specific?
- Where can achieve efficiencies by re-using modular IRT functionality?
- How can we streamlin IRT development from an internal-process perspective
- Can we really save time and effort by utilising preferred partnerships?