KREDO.TECH SERVICE PRICING
Medical Device Registration Costs
in Russia and the EAEU
From document preparation to full registration - all in one place
Document preparation, testing coordination, sample logistics, and regulator interaction - all the way through to your registration certificate
Reduced risk of rejection by Roszdravnadzor
Registration timeline shortened by 30-50%
Single point of accountability
Transparent regulatory process
Choose Your Cooperation Format
Starter
from USD 2,500
one-time fee
Ideal for companies entering the Russian market for the first time who need to understand registration pathways and document requirements.
- ✓ Technical dossier review
- ✓ Registration feasibility analysis
- ✓ Compliance gap report
- ✓ Registration pathway plan
- ✗ Full registration management
- ✗ Testing and logistics
Recommended
Basic
from USD 6,500
per registration project
Our most popular plan. We handle everything from document preparation to obtaining the registration certificate.
- ✓ Full technical dossier preparation
- ✓ Testing lab selection and coordination
- ✓ Sample logistics management
- ✓ Full regulator interaction
- ✓ Dedicated project manager
- ✓ Real-time progress tracking
Plan Comparison
| Included | Starter | Basic |
|---|---|---|
| Technical dossier review | ✓ | ✓ |
| Registration pathway planning | ✓ | ✓ |
| Full dossier preparation | - | ✓ |
| Testing coordination | - | ✓ |
| Sample logistics | - | ✓ |
| Regulator interaction | - | ✓ |
Client Choice
Why Most Clients Choose Basic
We take on all risks and communications - you just wait for the certificate
Fixed price, no hidden fees, full transparency throughout
Saves 6-12 months compared to handling registration independently
Dedicated project manager keeps you updated in real time
We Will Help You Choose the Right Plan
Answer a few questions in our Telegram bot and get a personalised recommendation
- What risk class is your device?
- Do you already have an authorised representative in Russia?
- What is your expected registration timeline?
What Affects Registration Costs
The final cost depends on a comprehensive assessment of several parameters:
- Device risk class (Class I, IIa, IIb, III)
- Whether clinical data or equivalence evidence is required
- Completeness of existing technical documentation
- Number and type of tests required
- Location and complexity of sample delivery
Ready to fast-track your registration?
Leave your contact details and our expert will get in touch within one business day.
