Find answers from
study documents.
Helping sites deliver high-quality research with confidence.
Helping sites deliver high-quality research with confidence.
Protocols and manuals are long. Key details are scattered. Ctrl+F only works when you already know the exact document and phrase.
Provide a summary of the study, including key inclusion/exclusion criteria for prescreening.
Is prednisone prohibited or restricted?
Are there special instructions that study participants should be aware of prior to study visit 2?
If a participant missed two doses of the investigational product, can treatment be resumed per the protocol?
What are the processing and shipping requirements for PK samples?
I have a monitoring visit — can you give me pointers to help me prepare?
What is the reporting timeline for suspected unexpected serious adverse reactions (SUSARs)?
What steps should I follow to complete study closeout?
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Peter is most helpful for verifying prohibited concomitant medications and exclusion criteria, especially when the lists are extensive.
Principal Investigator
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Like the mini protocols, Peter puts sponsor study documents at my fingertips. But, Peter helps me find information I need within seconds. This is revolutionary.
Clinical Research Coordinator
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New study onboarding is stressful. Quick access to the right info makes screening and randomization much more efficient and helps prevent mistakes.
Clinical Research Coordinator