The AI kit for Clinical Research Coordinators

Checks patient data against the protocol and drafts adverse event reports, SOPs and audit prep. Example: flagging a missed Visit 4 window.

Guides ethics review prep, consent forms, privacy and vulnerable population protections. Example: tightening a consent form's data sharing paragraph before IRB submission.

Researches regulatory requirements and drafts policies, risk registers and monitoring reports. Example: building a vendor risk register for a new lab.

Tracks new rules, compares them to your SOPs, drafts gap summaries and training. Example: new ICH guidance versus your monitoring SOP.

Like "Summarize Trial Inclusion Exclusion Criteria"

Like "Draft Clinical Trial Recruitment Copy"

Like "Explain Consent Sections In Plain Language"

Like "Build Participant Visit Schedule Template"

Every study visit is scheduled inside its protocol window with all prerequisites ready.

Every working file references the current approved protocol version, with procedure changes decided by the investigator.

Keep a complete, classified deviation log with each item followed to closure

The regulatory binder matches the sponsor checklist and is ready for sponsor review as early as possible.

Lets your AI search medical papers on PubMed and find clinical trials on ClinicalTrials.gov and ISRCTN.

Let your AI edit Word, PowerPoint and Excel files, with changes you can review before saving.

Let your AI search your Box files, answer questions about them, and pull out details for you.

Let your AI edit real Word documents: text, tables, tracked changes, citations and more.

Data Extraction transforms images and documents into organized, actionable data quickly and accurately, streamlining your workflow and saving time on manual dat

Redactable uses AI to identify and permanently remove sensitive information from documents, saving up to 98% time while ensuring data security for legal, health

Paperguide uses AI to simplify research by providing quick summaries, enabling efficient literature reviews, organizing references, and improving academic writi

RecordsKeeper.AI revolutionizes document management by merging AI and blockchain for secure, tamper-proof records. Automate classification, ensure compliance wi

Keeps every recorded deviation and its evidence in one traceable list, so monitoring visits start from facts, not memory.

Tracks approved visit windows and reminders so participants complete scheduled visits on time without extra chasing.

Keeps saved protocols, guidance and notes searchable with source and review state attached, cutting re-reading time.

Moves a question to a cited, reviewable report with sources and drafts kept in one place you own.

Search and retrieve clinical trial data from ClinicalTrials.gov API v2.

Query openFDA for drug, device, adverse event, recall, and regulatory data.

Writes clinical reports with regulatory compliance and validation tools.

Audits compliance across GDPR, HIPAA, SOC 2, PCI DSS, and ISO frameworks.