Standard annual plan
$15,000 / year
Billed annually, starting in Year 1.
All generally available standard modules, plus three clinical evaluation scopes, within your agreed contract scope.
Pricing · all prices in US dollars
One plan. The same price for every manufacturer.
Clinical evaluation is the core, not the whole subscription. The plan also covers Risk Management, GSPR and standards compliance, and PMS tracking, within the agreed availability and scope. Startups and established manufacturers get the same offer.
Your subscription
Choose how long you commit. Both options include the same features.
One subscription for the wider regulatory workload.
Clinical Evaluation, Risk Management, GSPR & Standards Compliance, and PMS Tracking.
All generally available standard modules are included—not sold as separate module plans. We confirm module availability and contracted limits before you sign.
See what each module covers ↓Three-year agreement
$10,000 / year
Billed each year, with a signed three-year agreement.
The same module coverage and three clinical evaluation scopes. Save $5,000 each year on the base subscription.
Add $2,500 once for implementation.
First-year total: $17,500 on the standard plan, or $12,500 with a three-year agreement.
These totals cover the base subscription and standard implementation for up to three scopes. Extra scopes and separately agreed services cost more.
Included module coverage
Clinical evaluation at the core. Risk, compliance and PMS alongside it.
The $15,000 annual subscription covers more than CER preparation. The goal is less repeated searching, copying and reconciliation across your regulatory workload. The $10,000 per year three-year option has the same module coverage.
All generally available standard modules are included within your agreement. We confirm the workflows, usage and support limits before you sign. Inclusion in the plan does not mean every planned workflow or cross-module connection is available today.
Part of the standard subscription
Clinical Evaluation
The core workflow: spend more time evaluating clinical evidence and less time assembling the same information for each report.
- Literature search strategy, screening and full-text appraisal
- Source-linked findings and review decisions
- Working literature-search reports, CEPs and CERs
Part of the standard subscription
Risk Management
Keep the risk assessment, controls and supporting references together instead of maintaining disconnected spreadsheets.
- Hazards, harm-specific assessments and initial/residual risk ratings
- Separate implementation and effectiveness evidence references
- Assessment history and readable Excel/PDF outputs
Part of the standard subscription
GSPR & Standards Compliance
Make it easier to see which requirements apply, why they apply and what evidence supports your response.
- GSPR checklists and standards compliance matrices
- Applicability, non-applicability and justifications
- Traceable implementation evidence and retained standard editions
Part of the standard subscription
PMS Tracking
Organize recurring post-market surveillance work around the findings and follow-up your team needs to review.
- Surveillance evidence, findings and reporting context
- Review of changes that may affect clinical or risk assessments
- Planned occurrence-band comparisons and human-reviewed risk-change proposals
PMS workflow availability is confirmed before contracting. Occurrence comparisons and change proposals are planned; risk records are not changed automatically.
Shared foundations. Your team stays in control.
Source references, evidence versions and review decisions support the work across these areas. Your team retains ownership of its information, makes the regulatory decisions and handles formal approval in its own quality process. Module inclusion is not a claim of automatic data transfer or regulatory compliance.
Standard implementation · $2,500 once
Setup, training and resources to get your team started.
Workspace setup
We create your manufacturer workspace and apply the standard configuration.
Three scopes set up
We set up your first three clinical evaluation scopes using the device information you provide.
60-minute kickoff
One remote session to agree on your starting point and next steps.
90-minute training
One remote session to show your team how to use the agreed workflow.
Guides and support materials
Standard onboarding guidance and reference materials for your team.
The implementation fee is separate from the subscription and is paid once. Your team provides the device information used for setup.
Your device portfolio
Three clinical evaluation scopes are included.
Three scopes is a clinical evaluation capacity allowance—not a limit of three modules. Risk Management, GSPR/standards and PMS are part of the same subscription, subject to agreed availability and module-specific limits.
What is a scope?
A scope is an agreed group of devices that share one Clinical Evaluation Report (CER) and its clinical evidence workflow.
It is not simply one model or catalog number. We agree the groups with you in the order form; unrelated devices need separate scopes.
$2,500 / year
For each scope beyond the three included.
Example: four scopes cost $17,500 per year on the standard plan, or $12,500 per year with a three-year agreement. Implementation is still $2,500 once.
Optional extras
Know what is quoted separately.
Historical document migration, custom integrations, bespoke configuration, regulatory consulting, CER authorship, extensive validation help and extra training are quoted separately.
Third-party standards and database licenses are extra where needed. We agree these costs with you before you commit.
Your team keeps responsibility for regulatory decisions and final document approval. Your signed agreement confirms the scope, usage and support limits, payment dates and termination terms.
Start with one recurring task
Is the recurring work costing your team too much time?
Pick the task that takes too much preparation. Walk through the Bevrik approach, confirm the available workflow and identify the review your team would still need to do.