Developed by a medical doctor with more than nine years in the pharmaceutical industry, to remove routine friction from document review, literature surveillance and regulatory analysis. All processing takes place locally in your browser: no uploads, no servers.
Every tool runs entirely in your browser. Your files never leave your device — critical when working with regulatory or clinical documents.
A complete PDF manipulation suite. Merge, split, stamp, watermark, rotate, convert, and compress — all offline.
Column-aware diff tool built for pharmaceutical inserts and regulatory documents with multi-column layouts.
Scan and analyse safety literature at scale — keyword-based or AI-assisted. Your text stays in your browser, or goes only to your chosen AI provider via your own API key.
AI-assisted safety literature analyser. Paste PubMed abstracts and get signal extraction, causality assessment, or PBRER-ready narratives — using your own API key.
Keyword-category highlighter for safety literature. Paste text, upload a PubMed .txt batch, import an Embase .xlsx export, or drop in a PDF — color-code signals, mechanisms, and populations at a glance.
injur catches injury, injured, injuriesTurn public regulatory datasets into answers for portfolio and generic-entry planning — parsed and filtered in your browser, exported to Excel in seconds.
Find FDA Orange Book patents expiring in any date window. Drop in the official products.txt and patent.txt files and get product- and patent-level results ready for Excel.
Planning tools for prioritising work and protecting time for high-value deliverables.
A strategic time manager that helps you identify your most important work, block your time, and track priorities — all in the browser.
Dr. Prashant Patel is a physician with an MD in Pharmacology and more than nine years in the pharmaceutical industry across pharmacovigilance, regulatory affairs and medical affairs.
Much of this work depends on dense documents: clinical study reports, SmPCs, patient information leaflets and regulatory submissions. Available tools are often costly, generic, or require confidential material to be uploaded to external servers.
These tools address specific gaps encountered in practice. Each runs entirely in the browser, with no installation and no data leaving the user's device.
No frameworks, no build step, no backend. Just the platform.
Three constraints shaped every decision.
Regulatory and clinical documents are confidential. Tools that require uploading them create avoidable risk, so everything here is processed locally within the browser.
No software installation, licences or IT onboarding. Each tool is a single page that can be bookmarked and used immediately.
Features reflect real working requirements, such as column-aware comparison for multi-column SmPCs, and prioritisation shaped by how medical and regulatory deliverables are managed.