Our plans
One plan per researcher profile
Try it for free. Buy a single synopsis, subscribe when projects pile up, or roll out Protocolis across your clinical research office teams.
The annual price only applies to the Solo subscription.
Discovery — try before you buy
no credit cardCreate an account and write one complete synopsis, in French or in English, for 7 days and with no credit card. Enough to judge Protocolis on a real project before choosing a plan.
Single synopsis
Ideal for 1 or 2 projects per year
€39.99
per synopsis · incl. VAT
- 1 complete synopsis (FR + EN)
- Import an existing synopsis
- PubMed + ClinicalTrials.gov analysis
- Regulatory roadmap
- Sourced regulatory chat
- Editable Word and PDF export
- Unlimited revisions · 30 days
- 12-month history
Solo
For very active investigators (9+ synopses per year)
€359.88
€249
per year · −31% (≈ €20.75/month)
- Everything in the single synopsis
- Unlimited synopses
- Your projects stay accessible after cancellation
- Synopsis versioning
- Standard email support
Team licence
Department, lab, research unit
€1,490
per year · excl. VAT · up to 10 named seats
- Everything in Solo × up to 10 users
- Team dashboard
- Workspace admin controls
- Protocol writing included
- Regulatory classification included
DRC/I (institution)
University hospitals, cancer centres, ESPIC, institutions
Custom quote
Essential 50 seats · Premium 150 seats
- Unlimited synopses and protocols
- Multi-project DRC/I dashboard
- Institution-specific protocol template
- Regulatory classification (included in Premium)
- Onboarding and team support
Prices in euros, including French VAT (20%). The Team licence is the exception: it is listed excluding VAT, as it is sold only to organisations that reclaim it.
Estimate your DRC/I's ROI
A simulator to build, task by task, the time drafting takes at your institution.
Add-on modules
Strengthen your plan with the regulatory modules
These modules complete your plan. They cannot be purchased standalone.
Regulatory classification
Decision tree for the French Loi Jardé (RIPH 1 / 2 / 3 / non-RIPH). Output: proposed classification, regulatory rationale and an exportable traceability document.
Included in DRC/I Premium and the Team licence · optional on DRC/I Essential
Regulatory FAQ
Targeted answers on RIPH/non-RIPH, Loi Jardé, the CPP ethics committee, the ANSM agency, health-data GDPR (MR-001 → MR-006), informed consent and academic sponsor status. Continuously updated.
Included in every plan, Discovery trial included
Frequently asked questions
Everything you want to know
Can I try before I buy?
Yes. The Discovery plan lets you write one complete synopsis, in French or in English, for 7 days and with no credit card. You then pick the plan that matches your project rhythm: pay-per-use, subscription, or institutional licence.
I already have a synopsis, can I import it?
Yes, on every plan and during the trial. Upload your Word or PDF document: Protocolis extracts what it contains, creates the study, and tells you which expected sections are still missing. You pick the writing up where it stands, instead of starting from a blank page.
Single synopsis or Solo subscription — how do I choose?
The single synopsis (€39.99 each) is the main offer, designed for occasional investigators (1-2 projects per year). The Solo subscription (€29.99/month or €249/year) only pays off above ~9 synopses per year — it is reserved for very active investigators, PhD students included. Clinical research associates and methodologists go through institutional licences. If you're unsure, start with single synopses and switch to Solo when needed.
When is the Team licence the right fit?
The Team licence (€1,490 excluding VAT per year for 10 users) is for a department head, lab or research unit that wants to equip its team without going through a full institutional procurement cycle. It can be purchased directly, no quote required. Above 10 users or for an institution-wide rollout, the DRC/I plan is a better fit.
What's included in the DRC/I plan?
Two tiers, both by custom quote (answer within 48 hours). DRC/I Essential (50 named seats) includes unlimited synopses and protocols, the DRC/I dashboard, the institution-specific protocol template and onboarding; regulatory classification and dedicated support are available as options. DRC/I Premium (150 named seats) includes everything in Essential, plus regulatory classification and dedicated support (CSM, 48h SLA).
How do the regulatory modules work?
The Regulatory FAQ is the regulatory chat: it is included in every plan, Discovery trial included. The Regulatory Classification module is included in the Team licence and in the DRC/I Premium licence, and available as an option on the DRC/I Essential licence.
Is my data secure?
Hosted in France, GDPR-compliant, encrypted in transit (TLS). None of your projects are used to train AI models. Legal notice and privacy policy are available in the footer.
How do I cancel my subscription?
In one click, from your account. Your data stays accessible for 30 days after cancellation so you can export anything you want to keep.
Another question? Contact us.