AVD Clinical unifies patients, CROs, sponsors, sites, and regulators through a single ecosystem — from study startup to closeout. Free resources today. Full platform coming.
Every essential clinical research template and SOP from TransCelerate, ICH, FDA, NIH, and EMA — organized in one place with AVD commentary. Sign in once and we'll email you when any of them update.
AVD Clinical creates a living ecosystem where every actor — patients to regulators — operates through one intelligent, secure, compliant system.
HIPAA-compliant portal, trial discovery, smart matching, health vault, ePRO, and emergency access — all on mobile.
Free to joinAI-powered patient pipeline, automated eligibility filtering, SOP tools, recruitment dashboards, and regulatory submissions.
$99–299/moMulti-study tracking, vendor comparison, budget automation, site performance AI, and enrollment forecasting.
$299–599/moROI dashboards, enrollment speed visibility, RFP portal, AI market intelligence, and cost transparency tools.
$499–999/moLean trial ops, adaptive design support, speed-to-IND tools, and access to enterprise-grade infrastructure at startup pricing.
Startup plansFHIR R4 integration bridge, EHR connectivity, automated source data verification, and zero-ETL pipelines.
API accessLicensed pharmacy verification, prescription validation, medication delivery integration, and refill reminders.
License verifiedCertifications, templates, AI tools, internship pipeline, and courses on digital clinical research.
$9–29/moThe pharmaceutical industry invests $50B+ annually in clinical research. The return is capped by a system built in the 1980s. Every year, the same failures repeat.
Poor site selection and manual recruitment processes cause delays worth billions in delayed drug approvals.
No visibility, travel burden, financial toxicity, and poor communication drive patients away before trials complete.
Manual SDV, fragmented systems, and duplicated effort across sites, CROs, and sponsors inflate costs at every step.
A system without unified data, AI automation, or real-time intelligence cannot move faster — until now.
Patients, sites, CROs, sponsors, EMRs, pharmacies, IRBs, and regulators each operate in completely separate systems.
Every competitor solves one slice. No one owns the connective tissue. That gap is exactly what AVD Clinical fills.
Explore the platform by stakeholder. Every feature is AI-powered, HIPAA-compliant, and designed for real clinical workflows.
Plain-language trial matching based on your health profile. No medical jargon. Multilingual. Connects to your EMR with consent.
↓ 60% screen failureAdaptive consent documents that adjust to your reading level and language. Comprehension checks built in. Full audit trail for regulators.
HIPAA · 21 CFR Part 11Upload medical records, prescriptions, vaccination history. Auto-visualizes your health timeline in charts. FHIR-native. Transfer data between portals for free.
Free 1st yearSmartwatches and health trackers sync automatically. Heart rate, steps, sleep, and glucose feed directly into your trial data — reducing manual ePRO burden.
Wearable-compatiblePregnancy tracker, period tracker, pediatric vaccine tracking, child development milestones, and sleep tracking — all private, all yours.
Daily engagementSmart medication reminders linked to your trial schedule. Verified pharmacy delivery integration with licensed pharmacy numbers. Prescription tracking and refill alerts.
License verifiedEnter study criteria — AI filters your consented patient pool and flags eligible subjects automatically. No more manual chart review.
↑ 40% recruitment speedReal-time enrollment tracking, pre-screening pipeline, consent status, and dropout risk scoring — all in one view for your whole site team.
Live dataAI-generated, GCP-aligned SOPs for site initiation, monitoring, data management, and pharmacy. Customized to your protocol. Fully audit-trailed.
GCP alignedAI calls, emails, or messages eligible patients, collects pre-screening answers, flags responders, and schedules site contacts — automated end-to-end.
Zero manual follow-upLive map of what major pharma companies and biotechs are building with AI in clinical trials. White spaces. Competitor moves. Trend signals.
Your Bloomberg terminalML model predicts site enrollment risk before activation using historical velocity, staff signals, and IRB timelines. Stop delays before they start.
↑ 40% on-time deliveryAI budget calculator with per-patient cost, monitoring cost, regulatory cost, and 10–15% contingency built in. RFP portal for vendor intake.
Free 1st reportAI drafts IND sections, clinical narratives, and protocol amendments. Cross-references FDA/EMA guidance and flags inconsistencies before submission.
↓ 70% prep time30+ professional-grade templates: SOPs, monitoring reports, feasibility checklists, communication plans, and budget sheets — all GCP-aligned.
From $19.99Digital Drug Development Essentials, AI in Clinical Trials, and the Digital Clinical Ops Certification — practical, on-demand, industry-recognized.
$49–199/courseEnter your protocol parameters — AI generates a complete, regulatory-compliant SOP. FDA and GCP-aligned language. Audit-ready output.
$9.99/monthBook a budget & feasibility snapshot with a clinical operations expert. High-ticket, high-value, remote. Starting at $650 per engagement.
From $650FHIR R4-native integration that opens 95% of US EHRs. AI maps non-standard data to CDASH/CDISC automatically.
FHIR R4 · 95% US EHRsAI reads source documents and auto-verifies against EDC entries. Flags data queries before monitors open the system. Reduces manual monitoring by 80%.
↓ 80% monitoring timePatients transfer reports, history, and records between hospitals, clinics, and countries with one click. Free for all patients. FHIR-compliant export.
Global portabilityAll physicians verified against official medical registries before platform access. Specialty tagging, institutional affiliation, and verified badge on profile.
Auto-verifiedClinical research is overdue for better tools. Sites still hand-build budgets in spreadsheets. CROs still chase paper templates across email threads. Sponsors still pay for the same SOP author trip three different times. Patients still struggle to find trials they qualify for.
AVD Clinical is building the resource layer first — a free library of curated regulatory references, a working budget calculator, and a growing set of original SOPs. The full operations platform comes next, in phases, with the same commitment: do the work in the open, be honest about what's built and what's coming, and never charge for what should be free.
Research, Innovation, Care — in that order.
No marketing fluff. If we don't have a feature yet, we say so.
Three things, all live: a free resource library with 40+ curated regulatory templates from TransCelerate, ICH, and FDA; a working AI Budget Calculator with sponsor and site-level estimation modes; and a growing pack of original AVD Clinical SOPs covering site, CRO, and sponsor activities. Everything else on our roadmap is clearly labeled "coming with platform launch."
Yes. Free, forever, with one-time sign-up (first name, last name, email, phone, role). Sign-up exists so we can notify you when source documents update — TransCelerate, ICH, and FDA push revisions multiple times a year. Your details are not sold. Unsubscribe any time.
The calculator uses industry-standard medians from published clinical trial budget references. It produces directional estimates within a reasonable range — useful for early planning, sponsor RFP responses, or site negotiations. It is not a substitute for a formal sponsor budget or a CRO bid. Real numbers vary based on protocol complexity, vendor mix, and contract negotiation. Use as a starting point, not a final answer.
No, and that's intentional. Our SOPs are starting frameworks with placeholders in square brackets that must be customized to your organization (sponsor name, effective date, document owner, local regulatory environment). Every SOP requires review by a qualified Quality Assurance professional before implementation. Anyone selling SOPs as drop-in-ready is misrepresenting what an SOP is.
Yes, any time. The Pro Monthly and Pro Annual subscriptions are processed through Gumroad. Open the receipt email from your purchase, click "Manage subscription," cancel. No questions, no retention calls, no friction. Annual subscriptions are non-refundable after 14 days but can be cancelled (you keep access until period end).
Not yet through self-serve checkout. For team licenses, SOP packs for an organization, or enterprise deployment of the upcoming platform, please contact us with your team size and needs. We respond within 1-2 business days.
Free resource library access (with sign-up). One-time reports or unlimited subscription for the AI Budget Calculator. Cancel anytime.
Join patients, researchers, sites, and sponsors already on the AVD Clinical waitlist.