The Clinical Trial Assistive Intelligence Device (Aide) Whose Time Is Now!
Picture this scenario – your PI is seeing a research participant for a scheduled visit. During the conversation, the participant shares that they have been experiencing muscle pain and asks if they can take ibuprofen. Given that the PI is working on a number of different protocols, they cannot remember if ibuprofen is an acceptable conmed. Instead of taking the time to search the 100+ page protocol, the PI simply poses this question to their AI chatbot. The correct answer is displayed immediately, how? First, the AI chatbot identified the biometrics of the PI as an authorized user for this particular protocol. Then, because the AI chatbot was pre-loaded by the sponsor with the protocol, the answer was easily retrieved. Time saved – correct information provided – communications and compliance improved – efficiencies increased!
But, don’t stop here – why not use the same technology for the benefit of the research participant wherever? Again, using the sponsor pre-loaded ICF, the AI chatbot can provide answers for the participant. And, if after seeing the answer, the participant still has questions, they can use the ICF embedded link to call the PI, if desired. Time saved – correct information provided – communications and compliance improved – efficiencies increased!
But wait, don’t stop here – why not use the same technology for the benefit of the sponsor/CRO monitor at their office to gauge site compliance with the protocol and GCP? Time saved – correct information provided – communications and compliance improved – efficiencies increased!
The QUALITY Equation
Quality = Time saved + correct information provided + communications and compliance improved + efficiencies increased + participant retention improved!
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