Use AI to research existing trials, analyze study designs, and write protocol sections with proper citations. Build stronger trial protocols more efficiently with comprehensive literature support.
Rated by 1000+ Researchers and Universities
Finding and reviewing relevant trials to support protocol design takes 2-3 months of searching.
Manually extracting study designs, endpoints, and methods from dozens of trials is time-consuming.
Creating background sections, study rationale, and methodology descriptions requires extensive literature review and citations.
Manual searches miss relevant trials that could inform better design decisions or safety considerations.
Without comprehensive evidence review, justifying design decisions like endpoints or criteria is difficult.
Ask questions about FDA, EMA, or other regulatory requirements for your therapeutic area. Get comprehensive answers with citations from official guidance documents.
Example: What are the FDA requirements for cardiovascular safety studies in diabetes drug development?
Use Literature Review to extract and compare study designs from multiple trials. See how other studies chose endpoints, inclusion criteria, and statistical methods.
Use AI Search to explore current research in your area and see what has been studied. Review the existing evidence to identify gaps and opportunities for your new trial, or use Deep Research to get comprehensive reports that highlight understudied areas.
Use AI Writer to generate background, rationale, and methodology sections with automatic citations. Get draft content that references relevant studies.
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Clinical Investigatorsdesigning new trials and writing study protocols
Protocol Writerscreating trial documents for regulatory approval
Regulatory Affairs Specialistspreparing drug applications and supporting documentation
CRO Teamsdeveloping protocols for pharmaceutical clients
Medical Writerscreating regulatory documents and clinical study reports
Biostatisticiansselecting study designs and statistical methods
Get comprehensive reports on therapeutic areas with detailed analysis of existing trials and gaps.
Compare trial designs across studies in organized tables with endpoint and safety data.
Ask specific trial design questions and get immediate answers with citations about optimal approaches.
Generate protocol sections like background and methodology with automatic references to relevant studies.
Ask questions directly to published trial protocols to understand specific design and methodology choices.
Create extraction forms for protocol elements like endpoints, populations, or methods for consistent comparison.