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Software + human expertise

A clear path from product evidence to reviewed documentation.

Get help defining your EU compliance scope, checking your declaration and organising the evidence behind it. Track the work, approve external testing and keep new product versions aligned in your private Cenitia project.

Request a scope review Track my service projects

Services are provided under a separate scoped order by Inovasense s.r.o. or an expressly identified specialist provider. The manufacturer retains statutory responsibilities.

Choose the level of support you need.

Indicative fees per agreed product family, excluding VAT. Models and versions, evidence readiness, review allowance and delivery timing are defined in your written quotation. Software subscription fees are separate unless the order explicitly includes them.

Subject to scope review

EU market readiness assessment

€199–290

one-off

Confirm the product, intended markets, relevant legislation and whether an EU representative is needed.

  • Written scope assessment
  • Evidence and testing gap list
  • Recommended next steps
Request this service
Subject to scope review

Declaration & evidence review

€590–890

one-off

A human review of your declaration, supporting reports, product identity, labels and instructions.

  • Annotated findings
  • Model and version consistency checks
  • One follow-up review of corrections
Request this service
Subject to scope review

Technical documentation project

€1,500–4,000

one-off

Organise existing evidence, prepare agreed documents and coordinate the missing evidence needed for your product.

  • Agreed technical-file sections
  • Traceable evidence index
  • Test plan and handover checklist
Request this service
Subject to scope review

Ongoing compliance support

€190–390

per month

Keep documentation aligned with agreed hardware and firmware changes, with scheduled expert reviews.

  • Scheduled review dates
  • Change and evidence review
  • Agreed consultation allowance
Request this service
Enquiry only

EU authorised representation

€1,990–2,990

per year + €690–990 onboarding

Enquire about a written mandate for selected electronic products. Appointment requires separate eligibility, legal and insurance approval.

  • Product-specific mandate assessment
  • Document availability and authority liaison
  • Corrective-action cooperation within the mandate
Discuss eligibility
Enquiry only

Medical device & AI specialist referral

Individual quotation

partner scope

Discuss a referral to a suitably qualified specialist. No partner appointment or representation is included in a software subscription.

  • Specialist scope assessment
  • Separate provider and commercial terms
  • Defined document handover
Discuss eligibility

Laboratory tests, notified-body assessments, translations, specialist legal advice and extensive corrective work are quoted separately. A document review or handover does not certify a product or guarantee authority acceptance. Representation requires a separately accepted written mandate; using the platform or sending an enquiry does not authorise use of our address on products.

Know what happens next.

  1. 1

    Tell us about your product

    Choose a service and describe the manufacturer, product family, versions and intended market. The enquiry is free and creates no appointment.

  2. 2

    Confirm the scope

    An expert checks suitability and requests the evidence needed to define the work. Upload confidential files only in your private project.

  3. 3

    Approve a written quotation

    Review the exact deliverables, exclusions, fee, VAT treatment, timing and service terms. Work starts after acceptance and payment confirmation.

  4. 4

    Complete the work and any testing

    Track questions and progress. External laboratory scope, sample requirements and additional costs need your separate approval before booking.

  5. 5

    Receive the reviewed handover

    Download findings and agreed deliverables, request corrections and record acceptance. A document handover is not a conformity certificate.

  6. 6

    Keep the product current

    For ongoing services, follow agreed review dates and submit hardware, firmware or market changes. Representation needs its own accepted written mandate.

External laboratory coordination

Cenitia does not operate a testing laboratory. Our engineering base in Trenčín gives us access to nearby testing providers. We select a laboratory for the exact product, standard edition, method and required scope; prices, sample handling and booking dates need written confirmation.

EVPÚ, a.s.

Nová Dubnica, Slovakia

Public information identifies EMC, electrical safety, climatic and mechanical testing. The exact standard edition, method and testing site must be confirmed for each project.

Candidate — no partnership or booking confirmed. Public sources checked 2026-10-07.

Provider informationPublished accreditation evidence

Technický skúšobný ústav Piešťany, a. s.

Piešťany, Slovakia

Public information identifies EMC, radio-equipment and electrical-safety testing. Specific methods, standard editions, current accreditation and capacity must be checked before booking.

Candidate — no partnership or booking confirmed. Public sources checked 2026-10-07.

Provider informationPublished accreditation evidence

Published capability is not confirmation of a partnership, available capacity or accreditation for every required test. Radio cybersecurity, chemical testing, batteries and specialised medical evidence may require additional providers.

Cenitia

The EU compliance engine for hardware manufacturers. Cited drafts, electronic signing, regulation watching — all in one place.

A product of Inovasense s.r.o., Bratislava, Slovakia · Data hosted in Stockholm, EU

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Operated in Slovakia · Evidence, expert review and clear service scope