Free curated regulatory templates, an AI-assisted trial budget calculator, and original SOPs — built for sites, CROs, and sponsors who need real answers today, not a roadmap.
✓ Live right now — no waitlist: Resource Library · Budget Calculator · SOP Templates
Industry-cited estimates from publicly available clinical trial research; figures vary by source and study.
Clinical trials don't have to run on spreadsheets, email threads, and institutional memory. Watch an overview of what modern trial operations look like — and what AVD Clinical is building toward.
We believe in transparency. Here's exactly where AVD Clinical is today.
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.
From free SOPs to full platform access. Secure checkout powered by Stripe — AVD Clinical never sees or stores your card details.
See all plans including SOP Unlimited ($99/mo) and Calculator Unlimited ($19/mo or $149/yr) → Full Pricing Page
The Library, Calculator, and SOPs above are live today. Everything below is the platform we're building toward — shown here so you know what's coming, not so you think you can buy it yet.
HIPAA-aligned design, trial discovery, study matching support, health information vault, and patient-controlled emergency profile — all on mobile.
Planned · free to joinAI-assisted patient pipeline, eligibility screening support, SOP tools, recruitment workflow tracking, and regulatory document management.
Planned · $99–299/moMulti-study tracking, vendor comparison, budget automation, site performance AI, and enrollment forecasting.
Planned · $299–599/moROI dashboards, enrollment speed visibility, RFP portal, AI market intelligence, and cost transparency tools.
Planned · $499–999/moLean trial ops, adaptive design support, speed-to-IND tools, and access to enterprise-grade infrastructure at startup pricing.
Planned · startup plansFHIR-ready interoperability planning, EHR connectivity design, source data review support, and data integration workflows.
Planned · API accessLicensed pharmacy verification, prescription validation, medication delivery integration, and refill reminders.
Planned · license verifiedCertifications, templates, AI tools, internship pipeline, and courses on digital clinical research.
Live now · from $19/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.
Few platforms connect patients, sites, CROs, sponsors, and operational workflows in one AI-enabled layer. That gap is exactly what AVD Clinical fills.
Figures above are industry-cited estimates from publicly available clinical research sources; actual figures vary by study and publication.
Every card is labeled so you know exactly what you can use today vs. what's on the roadmap. We build in phases and we don't pretend otherwise.
Set reminders for your own medications — name, dose, prescribing doctor, pharmacy, refill date, and notes. Encrypted and private. Browser-based push notifications.
Free · No PHI acceptedPregnancy tracker, period tracker, pediatric vaccine tracking, child development milestones, and sleep tracking — personal health tools, not clinical data collection.
In developmentPlain-language trial matching based on your health profile. Multilingual. Connects to your EMR with consent. Requires validated backend and BAA framework — not currently available.
Future platformAdaptive consent documents with comprehension checks and a full 21 CFR Part 11 audit trail. Requires validated electronic signature infrastructure — not currently available.
Future platformUpload and store medical records, prescriptions, and vaccination history. FHIR-ready export design. Requires HIPAA BAA infrastructure — not currently available.
Future platformSmartwatch and health tracker sync feeding directly into trial data to reduce manual ePRO burden. Requires device API partnerships and validated data pipeline — not currently available.
Future platformGCP-aligned SOPs, monitoring report templates, site initiation checklists, and data management forms — download-ready frameworks you adapt to your protocol. Requires your QA review before operational use.
Available now · From $19Enter study criteria — AI filters your consented patient pool and flags eligible subjects. Requires access to patient records and consent infrastructure — not currently available.
Future platformReal-time enrollment tracking, pre-screening pipeline, consent status, and dropout risk scoring. Requires integrated site data feeds — not currently available.
Future platformAI-assisted coordinator outreach, pre-screening data collection, and responder flagging — subject to consent and human oversight. Requires validated CRM integration — not currently available.
Future platformPer-patient cost, monitoring cost, and regulatory cost modelling across countries and site configurations. Export to PDF or Word. Free first calculation.
Free · Available nowCompetitive intelligence on what major pharma and biotechs are building with AI in clinical trials. Requires live data licensing and analyst infrastructure — not currently available.
Future platformML model predicting site enrollment risk before activation. Requires historical site performance data at scale — not currently available.
Future platformAI-assisted drafting of IND sections, clinical narratives, and protocol amendments with FDA/EMA guidance cross-referencing. Requires validated regulatory submission pipeline — not currently available.
Future platform30+ professional-grade templates: SOPs, monitoring reports, feasibility checklists, communication plans, and budget sheets — all GCP-aligned. Download and adapt to your organization.
From $19 · Available nowBudget & feasibility snapshot with a clinical operations expert. Remote. Limited availability — contact us to enquire.
From $650 · Contact usEnter protocol parameters — AI generates a customizable SOP framework with GCP-aware language. Output requires QA and legal review before regulated use.
In developmentDigital Drug Development Essentials, AI in Clinical Trials, and the Digital Clinical Ops Certification — practical, on-demand, industry-recognized.
In developmentFHIR R4-aligned connectivity with US EHRs and CDASH/CDISC data mapping. Requires validated integration layer and enterprise agreements — not currently available.
Future platform · Enterprise onlyAI-assisted source document review to identify discrepancies against EDC entries and support query flagging. Requires access to trial data systems — not currently available.
Future platform · Enterprise onlyPatient-controlled transfer of health records and history between providers and countries with consent. FHIR-ready export design. Requires HIPAA BAA framework — not currently available.
Future platformPhysician verification against official medical registries with specialty tagging and institutional affiliation. Requires registry API partnerships — not currently available.
Future platformClinical 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. All subscriptions are processed securely through Stripe. To cancel, log in to your account, go to billing, and cancel — or email [email protected] and we'll handle it within one business day. 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.
Whoever you are in clinical research, there's a free starting point waiting for you right now.