Risk-linked enrolment
Role, site and exposure information determine the appropriate health activity. Changes create review work rather than silent alterations.

For manufacturing organisations
Manufacturing health risks depend on task, process and exposure duration. Occentra connects role and risk information to programme requirements so surveillance follows actual work.
Risk-based model
Job titles do not always describe actual exposure. When people change line or shift, requirements should update accordingly.
Role, site and exposure information determine the appropriate health activity. Changes create review work rather than silent alterations.
Noise, vibration and respiratory records are meaningful as a sequence. Earlier results and work context inform clinical interpretation.
Assessments fit production and availability across early, late and night shifts. Missed appointments are visible, not assumed.
Restrictions concern specific tasks: machinery, driving, respiratory equipment. Managers receive functional advice and review date.
Programme coordination
Noise, vibration and respiratory surveillance can run independently while connecting to the same person.
Audiometry, questionnaires, clinical review and recall. Thresholds trigger escalation for professional attention.
Staged pathway for vibration exposure. Questionnaires, tier assessment and clinical escalation coordinated.
Spirometry, questionnaires and follow-up for relevant exposures. Previous results available for trend review.
Functional and clinical evidence for machinery, vehicles or defined risk. Restrictions and review periods recorded.
Exposure continuity
Role changes should update requirements without losing earlier history.
A practical example
Updated role or risk information indicates a new surveillance pathway. OH sees the requirement alongside existing history.
The employee is scheduled into a shift-accessible appointment. Pre-assessment information and previous results are available to the practitioner.
Assessment is recorded in a structured template. Findings meeting escalation criteria are routed for clinical review.
Management advice about work or controls is released through a protected process. Managers receive functional action, not the medical record.
Programme reporting shows completion and whether follow-up remains outstanding.
What changes
Earlier visibility of gaps, less manual reconciliation. Workplace controls and clinical decisions stay with competent people.
Due, overdue and incomplete activity visible by programme and site. Missing role data, non-attendance and clinical review treated as different problems.
Earlier assessments and work context stay connected when people change role or site. Practitioners gain a clearer longitudinal view.
Shift-aware scheduling and visible appointment status help plants coordinate release. Missed work identified before the next review.
Authorised reports state restrictions and control advice in practical terms. Supervisors act without unnecessary clinical information.
Why Occentra
Occentra models referrals, cases, appointments and reports around the work occupational health actually does. Configuration adapts the platform to different organisations without creating separate software branches.
Draft, submitted, received, triaged and accepted are distinct states. Teams can see what is ready for clinical work and what needs attention first.
Tasks, appointments and forms connect to the employee and referral. A case stays open while scheduled work or review actions remain.
Teams publish versioned templates. Submitted answers stay tied to the form used, while new work moves to the current version.
Operations, advisers, physicians and managers receive different abilities. Server-side checks keep those boundaries consistent.
Explore Occentra
Review the platform from the commercial, operational and architectural angles that matter to your buying team.
Understand scope and commercial fit.
Compare approaches to OH software.
See the occupational health work Occentra supports.
See how Occentra fits your systems.
Related solutions
Keep questionnaires, assessments, outcomes and history connected for people who need ongoing workplace health checks.
Receive, triage and accept requests for occupational health input, then continue the work in a connected case.
Move pre-employment questionnaires through review, clinical assessment where needed, and an occupational health outcome.
Frequently asked questions
Yes. Each has its own form, clinical review route and recall period. Employees can belong to more than one programme. Submitted assessments stay tied to the form version used.
No. The employer's competent risk assessment sets the requirement. Occentra records who is enrolled, which pathway applies and when the next assessment is due.
Yes. Submitted forms remain on the employee's history with date and version. Clinicians review the sequence; supervisors receive only programme status and authorised advice.
Appointments are organised by plant, practitioner, time and method in one diary. Occentra checks for clashes and distinguishes completed, cancelled and did-not-attend bookings.
Yes. Sites use different locations, forms and lookups where risks genuinely differ. Employee, referral and appointment states remain consistent for comparable reporting.
The authorised fitness advice, restriction, programme status and review date. Questionnaire answers, test results and medical records stay restricted to OH.
Other industries
Manage mobile workforces, contractors and safety-critical assessments across changing sites.
Coordinate driver fitness, depot health programmes and return-to-work advice across national networks.
Run multi-client referrals, clinical cases, appointments and reporting from one governed platform.
Book a walkthrough around your sites, shifts, exposure-led surveillance and safety-critical work. We show the path from programme requirement to authorised outcome.