CONNECTED MODULES. CONSISTENT CONTROL.

Connected modules for hospital records, traceability and resources

Jovimed modules cover usage and audit registries, sterilisation traceability, biocide records, predictive inventory, equipment and staff. Daily operational stock and disaster reserves have separate records. Specialist workflows add infection surveillance, accreditation evidence, CNAS reimbursement support and hospital continuity planning.

EXTEND OPERATIONAL CONTROL

Ten perspectives. One hospital.

Explore workflows for patient safety, revenue protection and continuity. Each module follows its own path from the first signal to action and evidence.

CLINICAL SAFETY

Infection Surveillance & Antimicrobial Stewardship

Electronic infection records, microbiology and responsible antimicrobial use, connected through clinical review.

Explore the module
QUALITY AND CLINICAL RISK

Patient Safety, Clinical Risk & Accreditation

Incidents, clinical risks, corrective actions and accreditation evidence with clear ownership.

Explore the module
OPERATIONS AND ENVIRONMENT

Medical Waste Traceability & Reporting

Waste categories, quantities, handovers and disposal documentation in one traceable history.

Explore the module
FINANCIAL AND CLINICAL CONTROL

CNAS Reimbursement Evidence & Revenue Protection

Connect services, documentation and consumption to review reimbursement evidence and protect legitimate revenue.

Explore the module
DEVICES AND SAFETY

Implant Traceability & Recall Management

UDI identifiers, procedures and patients connected for review and safety follow-up.

Explore the module
COOPERATION & RESILIENCE

Regional Hospital Mutual Aid Network

Partner-confirmed capacity, assistance requests and resource transfers tracked through to completion.

Explore the module
REGULATORY INTELLIGENCE

Regulatory Change Impact Engine

From official legislation to updated procedures, training and evidence, with human review and approval.

Explore the module
OPERATIONAL PREPAREDNESS

Hospital Rehearsal Simulator

Disruption scenarios, interdependent resources and response plans compared before a real event.

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DIGITAL RESILIENCE

Clinical Cyber Continuity Map

Digital dependencies, fallback procedures and recovery priorities connected to clinical impact.

Explore the module
STAFF HEALTH

Occupational Health Surveillance

Role- and exposure-specific examinations, restricted medical results and administrative reminders for management.

Explore the module

The operational foundation.

The registries, stock, equipment and access controls connecting everyday work.

COMPLIANCE

Registries and audit

Usage registries, supporting documents and action histories, organised for inspections and audits.

Sterilisation traceability01
Accreditation evidence02
Occupational health03

Illustrative data

Digital recordsResponsibilities
TRACEABILITY

Sterilisation and biocides

Follow sterilisation kits, cycles and their use. Keep clear records of biocide solutions and checks.

Kit identified
Cycle tracked
Use recorded
Kits and cyclesBiocide registries
RESOURCES

Inventory and reserves

Daily and predictive stock management for medication and supplies. Everyday inventory and national disaster reserves have separate records.

Available stock forecast

units
Illustrative stock: from 320 to 184 units over seven days.
RecordedForecastForecast range

Illustrative stock: from 320 to 184 units over seven days.

Example forecast; these values do not come from a hospital.
View example data
PeriodunitsForecast range
Mon320
Tue298
Wed274
Thu251
Fri228211–245
Sat204181–227
Sun184154–214
Batches and expirySeparate reserves
CONTINUITY

Equipment and maintenance

Medical machinery and equipment records, inspection schedules and planned interventions, with visibility into available resources.

Equipment inventory
Next inspection
Maintenance history
InspectionsUsage history
TEAMS

People and workplace safety

Occupational health, employee records, checks and training. Alerts for deadlines, fire extinguishers and safety documentation at each location.

Clear responsibilities across every team.
TrainingExpiry alerts
GOVERNANCE

Roles and permissions

Access matched to roles and responsibilities. The right people see relevant information and approve the actions assigned to them.

View Update Approve
Granular accessHuman approval

SEE HOW IT WORKS

Follow one problem through to action.

Choose an example and watch how information moves between people, records and decisions. Explore each step at your own pace.

JOVIMED / 01Illustrative example

Proposed actions keep their source reference and pass through human review.

From an amended provision to an approved plan.

Imagine a sterilisation requirement changes. Follow the source through the teams, proposed tasks and evidence it may affect.

  1. See exactly what changed.

    The amended wording is compared with the previous version. The official publication, article and relevant dates stay attached so the team can verify the change.

    The team can check the original provision before deciding what it means.

  2. Find the teams and procedures that may be affected.

    AI connects the provision to the hospital's configured departments, procedures, equipment and training. Responsible people check whether each suggested connection applies.

    A legal change becomes a focused review for the people it may concern.

  3. Turn the reviewed impact into proposed tasks.

    The engine proposes procedure updates, training and evidence to collect. Each proposal includes its source reference, relevant deadline and a suggested owner for review.

    Each proposed task explains what to change, why and who could own it.

  4. Approve the plan, then keep proof of completion.

    The responsible team checks and approves the plan. Assigned owners update documents and record training, linking completion evidence back to the approved action and original source.

    Reviewers can follow the path from legal source to approval and implementation.

Why this matters
JOVIMED / 02Illustrative example

Clinical references are visible only to authorised teams.

One lot number connects receipt, use and follow-up.

Follow an illustrative implant lot from delivery to a recall notice. See how its identifiers help authorised teams find the records that need review.

  1. Give the received implant a traceable identity.

    The team records the available UDI, lot or serial number and links the supplier's receipt documents. These identifiers connect the device to its later movements.

    The identifier provides a starting point for tracing the device's history.

  2. Connect the device to the procedure where it was used.

    The authorised clinical team links the implant identifier to the procedure and patient reference. Access controls protect the clinical information associated with that record.

    The hospital can trace use without exposing patient details to every user.

  3. Match a verified notice against stock and procedure history.

    A recall notice identifies the lot. Matching identifiers reveal remaining stock and linked procedure records for review by authorised teams, including the associated patient references.

    The same lot number connects unused devices and records of devices already implanted.

  4. Record stock controls and clinician-led follow-up.

    Responsible staff document quarantine of affected stock as required by the notice. Clinicians determine patient assessment and communication, with restricted access to follow-up records and completion evidence.

    Stock actions and clinical follow-up remain distinct, assigned and documented.

Why this matters
JOVIMED / 03Illustrative example

National disaster reserves remain separate and are not shared automatically.

From a shortage to an agreed, traceable transfer.

A hospital needs emergency supplies from a participating partner. Follow the request through availability checks, approvals, delivery and replenishment.

  1. Describe the shortage and when help is needed.

    The requesting hospital specifies the supplies, quantity, urgency and transport requirements. A named coordinator owns the request so potential partners have a clear point of contact.

    Partners can assess a concrete request instead of an incomplete message.

  2. Check which partner can actually release suitable supplies.

    The network matches the request to participating hospitals' offers. The supplying team confirms current availability, compatibility, release conditions and when the offer was last checked.

    A listed offer becomes usable only after the partner confirms it.

  3. Both hospitals approve the terms before anything moves.

    Authorised people at both hospitals approve quantities, transport, handover and replenishment responsibilities. Resources governed by special rules follow their applicable release approvals and agreements.

    The transfer begins with shared terms and named responsibilities.

  4. Track dispatch, receipt and what must be replenished.

    Teams record identifiers, quantities and handovers, then check receipt against dispatch. Discrepancies and replenishment deadlines remain linked to the request until the agreed obligations are completed.

    Delivery and replenishment have a visible record, owner and completion status.

Why this matters

Illustrative scenarios with fictional records. People review and approve the actions shown.

FROM A SIGNAL TO A CLEAR NEXT STEP

Explore a working day.

See how connected information can support an operational discussion. These are illustrative workflows to explore in a demonstration.

Illustrative workflow

An auditor asks for a kit’s history.

Bring the registry, supporting documents and responsible people into the same discussion.

  1. Signal

    A request arrives for a specific sterilisation kit.

  2. Context

    Review the kit identifier, linked cycle and usage record.

  3. Human decision

    An authorised colleague reviews gaps and assigns follow-up.

  4. Recorded evidence

    Keep the supporting record, action owner and review history together.

What becomes clearer

A clear route from an audit question to an owner and supporting evidence.

Explore this scenario in a demo

Evidence to follow

  • Kit and cycle identifiers
  • Usage registry entry
  • Review owner and action history

Illustrative workflow

A daily-use batch is approaching expiry.

Consider consumption and availability while keeping the emergency reserve distinct.

  1. Signal

    A batch-expiry alert calls for attention.

  2. Context

    Compare the batch with operational demand and separately recorded reserves.

  3. Human decision

    An authorised person considers the appropriate stock action.

  4. Recorded evidence

    Record the decision, responsible person and inventory movement.

What becomes clearer

Daily availability and disaster reserves remain separate in the decision.

Explore this scenario in a demo

Evidence to follow

  • Batch and expiry information
  • Operational stock record
  • Separate reserve record and approved action

Illustrative workflow

Equipment and team deadlines converge.

Bring the upcoming inspection and training into view before planning the next activity.

  1. Signal

    An equipment inspection and a training deadline approach.

  2. Context

    Identify the affected equipment, team and location.

  3. Human decision

    Assign responsibilities and agree the follow-up with the relevant people.

  4. Recorded evidence

    Record completion and link the supporting documents.

What becomes clearer

Deadlines become named actions that the manager can follow.

Explore this scenario in a demo

Evidence to follow

  • Equipment record and inspection date
  • Training or occupational health record
  • Owner, completion and supporting document

IN PRACTICE

Questions about hospital modules

Are everyday stock and disaster reserves tracked separately?

Yes. Separate records distinguish everyday consumption from emergency availability. Resource categories, responsibilities and approvals are configured according to the rules governing each resource.

What do the sterilisation and biocide workflows track?

The workflows follow sterilisation kits, cycles and recorded use alongside biocide solutions and checks. These records support traceability and the preparation of evidence for audit.

How are workplace safety training and deadlines monitored?

Jovimed connects staff, training, examinations and site documentation with owners and due dates. Notifications highlight reassessments, inspections and expirations that require action.

START WITH A CLEARER PERSPECTIVE

Let’s talk about
your hospital.

Discover how registries, traceability and resource management fit into the way your team works.

Request a demo A conversation about your processes and priorities.office@jovimed.ro
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