{{org_field_logo}}
{{org_field_name}}
Registration Number: {{org_field_registration_no}}
Sharps and Needlestick Injury Policy
1. Purpose
The purpose of this policy is to provide clear, comprehensive, and up-to-date guidance on the safe handling and disposal of sharps, and the management of needlestick and sharps-related injuries within {{org_field_name}}. As a temporary staffing agency supplying registered nurses and healthcare assistants to care homes and other healthcare settings, {{org_field_name}} recognises its legal and moral duty to protect staff, service users, and others from the risks associated with sharps and needlestick injuries. This policy sets out the procedures that all staff must follow to minimise the risk of injury and blood-borne virus (BBV) transmission, and to comply with national legislation and best practice guidance.
This policy has been prepared with reference to the Health and Safety at Work etc. Act 1974; the Management of Health and Safety at Work Regulations 1999; the Control of Substances Hazardous to Health Regulations 2002; the Health and Safety (Sharp Instruments in Healthcare) Regulations 2013; the Personal Protective Equipment at Work Regulations 1992, as amended; the Reporting of Injuries, Diseases and Dangerous Occurrences Regulations 2013; the Safety Representatives and Safety Committees Regulations 1977; the Health and Safety (Consultation with Employees) Regulations 1996; the Employment Agencies Act 1973; the Conduct of Employment Agencies and Employment Businesses Regulations 2003; the UK General Data Protection Regulation; the Data Protection Act 2018, as amended by the Data (Use and Access) Act 2025; and relevant guidance issued by the Health and Safety Executive, the UK Health Security Agency and the Department of Health and Social Care.
{{org_field_name}} is an employment business supplying temporary healthcare workers. It does not itself provide or manage regulated care and is not relying on this policy as evidence that it carries on a regulated activity requiring registration with the Care Quality Commission. Workers must nevertheless follow lawful local infection-prevention and sharps procedures operated by the healthcare provider at each placement.
2. Scope
This policy applies to:
- all registered nurses, nursing associates, healthcare assistants and other temporary workers supplied by {{org_field_name}} who may use, handle, dispose of or otherwise come into contact with medical sharps, blood, body fluids or contaminated equipment;
- all employees, directors, consultants and office-based personnel who arrange placements, assess placement suitability, investigate incidents or support affected workers;
- all placements in care homes, nursing homes, hospitals, clinics, community services and other healthcare or social-care environments where exposure to sharps may reasonably occur; and
- sharps injuries, bites resulting in blood exposure, splashes to the eyes or mouth, and blood or body-fluid contact with broken or damaged skin.
This policy applies alongside the placement provider’s health and safety, infection-prevention, clinical-waste, occupational-health and incident-reporting procedures. Where the placement provider’s procedure imposes a higher standard of protection, the higher standard must be followed, provided it is lawful and has been communicated to the worker.
{{org_field_name}} and the placement provider must co-operate and exchange sufficient information to manage the worker’s health and safety. The placement provider ordinarily controls the premises, equipment, local working environment, supervision and immediate emergency arrangements. {{org_field_name}} remains responsible for the matters within its control, including suitable worker selection, provision of information, confirmation of competence, escalation, worker support and monitoring of placement safety.
3. Related Policies and Procedures
This policy should be read together with the following:
- Infection Prevention and Control Policy;
- Health and Safety Policy;
- Incident, Accident and Near-Miss Reporting Policy;
- Risk Assessment Policy;
- Occupational Health and Fitness-to-Work Policy;
- Immunisation and Health Screening Policy;
- Personal Protective Equipment Policy;
- Clinical Waste and Waste-Disposal Policy;
- Training, Competency and Supervision Policy;
- Data Protection and Confidentiality Policy;
- Worker Wellbeing and Post-Incident Support Policy;
- Whistleblowing Policy;
4. Policy Statement
{{org_field_name}} will take all reasonably practicable steps within its control to prevent injury and infection arising from medical sharps and occupational exposure to blood or other potentially infectious material.
In particular, {{org_field_name}} will:
- seek to ensure that workers are placed only in environments in which foreseeable sharps risks have been assessed and suitable control measures are available;
- obtain relevant health and safety information from the placement provider before or at the start of an assignment;
- confirm that workers have received suitable information, instruction and training for the tasks they are expected to perform;
- ensure that workers understand how to obtain immediate first aid, clinical risk assessment, occupational-health advice and post-exposure treatment;
- require workers to report sharps injuries, blood or body-fluid exposures, unsafe practices and near misses without delay;
- co-operate with placement providers in investigating incidents and implementing corrective action;
- protect the confidentiality of workers’ medical and occupational-health information; and
- ensure that no worker is subjected to detriment for reporting a genuine safety concern or refusing work which they reasonably believe presents serious and imminent danger.
Workers must use medical sharps only where they are competent, authorised and acting within their professional scope of practice and the placement’s documented procedures.
5. Responsibilities
5.1 Directors
The directors of {{org_field_name}} will:
- retain overall accountability for this policy;
- appoint a competent person to oversee sharps safety and occupational-exposure arrangements;
- provide sufficient resources for training, occupational-health support, investigation and corrective action;
- establish arrangements for access to urgent clinical advice during and outside normal office hours;
- monitor compliance, incident trends, client performance and lessons learned; and
- ensure that significant or repeated placement failures are escalated and, where necessary, that workers are withdrawn from unsafe placements.
5.2 Health and Safety Lead or Clinical Lead
The designated Health and Safety Lead or Clinical Lead will:
- maintain this policy and associated procedures;
- review sharps-related risk information received from placement providers;
- support incident investigation and determine whether external reporting may be required;
- liaise with occupational health, the placement provider and the affected worker;
- ensure that corrective actions are allocated and completed;
- monitor immunisation, training and competency arrangements at an organisational level without unnecessarily accessing detailed confidential clinical information; and
- advise directors when a placement should be suspended or terminated on safety grounds.
5.3 Recruitment and Placement Personnel
Recruitment and placement personnel will:
- obtain information from the placement provider about the work, known hazards, safer-sharps arrangements, required competence, PPE, emergency procedures and occupational-health contacts;
- provide the worker with relevant placement information before the assignment begins;
- ensure that the worker’s qualifications, experience, training and declared competence are appropriate for the proposed duties;
- avoid placing a worker in a role involving sharps where required training or competence has not been demonstrated; and
- record and escalate any concerns raised by the worker or placement provider.
5.4 Placement Provider or Hirer
Before accepting or continuing a placement, {{org_field_name}} will seek written confirmation that the placement provider:
- has assessed the risks arising from medical sharps and exposure to biological agents;
- avoids unnecessary use of sharps and uses safer sharps so far as reasonably practicable;
- supplies suitable equipment, PPE and secure sharps containers close to the point of use;
- provides local induction, information, instruction, supervision and emergency procedures;
- maintains suitable first-aid and occupational-exposure arrangements;
- reports and investigates incidents for which it is the responsible person;
- informs {{org_field_name}} promptly of any incident involving an agency worker; and
- co-operates in providing information reasonably required for investigation, medical risk assessment and legal reporting.
5.5 Agency Workers
Agency workers must:
- follow this policy and the placement provider’s lawful local procedures;
- work only within their competence, authorisation and professional scope of practice;
- inspect equipment before use and report damaged, inappropriate or unavailable safety equipment;
- use safer-sharps features correctly and never deliberately disable them;
- dispose of sharps immediately and safely;
- report injuries, exposures, near misses and unsafe practices without delay;
- attend occupational-health assessment and follow-up where reasonably required;
- co-operate with incident investigations; and
- stop the task and seek assistance where there is an immediate risk of serious injury or where appropriate equipment, training or disposal facilities are unavailable.
6. Definitions
For the purposes of this policy:
Medical sharp means an object or instrument required for a healthcare activity which can cut, prick or otherwise cause injury. It includes needles, syringes with attached needles, cannulae, scalpels, lancets, stitch cutters, blades and other sharp medical instruments.
Safer sharp means a medical sharp designed and constructed with an integrated safety feature or mechanism which prevents or minimises accidental cutting or skin puncture.
Sharps injury means any cut, puncture, scratch or other injury caused by a sharp. For legal purposes under the Sharps Regulations, injury includes infection.
Occupational exposure incident includes:
- puncture or injury from a used or potentially contaminated sharp;
- blood or potentially infectious body fluid splashed into the eye, mouth or nose;
- blood or potentially infectious body fluid contacting broken, inflamed or damaged skin; and
- a human bite which breaks the skin or results in blood exposure.
Blood-borne virus means a virus transmitted through blood or certain body fluids, including hepatitis B, hepatitis C and human immunodeficiency virus.
Broken glass and other non-medical sharps are covered by the general duties under health and safety and COSHH legislation, even where they do not meet the specific definition of a “medical sharp” under the Health and Safety (Sharp Instruments in Healthcare) Regulations 2013.
7. Hazards Associated with Sharps and Blood Exposure
Sharps injuries and occupational exposure incidents may result in:
- transmission of hepatitis B, hepatitis C, HIV or other infectious agents;
- local or systemic bacterial infection;
- cuts, puncture wounds, scarring or other physical injury;
- anxiety, distress, sleep disturbance or other adverse psychological effects;
- side-effects from post-exposure medication;
- time away from work and disruption to professional duties; and
- risks to service users and others where contaminated sharps are not controlled.
Circumstances increasing risk include:
- recapping or manipulating used needles;
- failure to activate a safety mechanism;
- overfilled, incorrectly assembled or poorly positioned sharps containers;
- carrying used sharps to a remote disposal point;
- passing sharps directly from hand to hand;
- unexpected movement by a service user;
- inadequate lighting, space, staffing or supervision;
- rushed, fatigued or interrupted working;
- lack of competency or local induction; and
- failure to follow standard infection-control precautions.
8. Risk Assessment and Placement Suitability
{{org_field_name}} will assess the sharps-related risks within its control and will obtain sufficient information from the placement provider to determine whether the proposed work is suitable for the worker.
Before deployment, or as soon as reasonably practicable where an urgent placement is accepted, {{org_field_name}} will seek information about:
- the nature of the clinical tasks and whether medical sharps will be used;
- the types of sharps and safety-engineered devices provided;
- the placement provider’s sharps and COSHH risk assessments;
- local disposal facilities and waste arrangements;
- the PPE required;
- known behavioural or environmental risks;
- the training, qualifications and competencies required;
- first-aid, occupational-health and out-of-hours exposure procedures; and
- the identity of the person responsible for reporting and investigating incidents.
Risk assessments must consider the hierarchy of control and must:
- avoid the use of medical sharps where reasonably practicable;
- use safer sharps where reasonably practicable;
- provide suitable equipment, staffing, space, lighting and supervision;
- place clearly marked, secure sharps containers close to the point of use;
- prevent unauthorised access to sharps and sharps containers;
- provide suitable PPE where residual risks remain;
- address foreseeable emergencies, challenging behaviour and lone working; and
- consider workers who may be particularly vulnerable because of pregnancy, disability, inexperience, language needs or other relevant circumstances.
The risk assessment must be reviewed where:
- a sharps injury, exposure incident or near miss occurs;
- a safer device fails or is used incorrectly;
- work activities, equipment or placement conditions change;
- a worker raises a concern;
- monitoring identifies a pattern of incidents; or
- new legislation or authoritative guidance is issued.
9. Information Before Placement
Before a worker undertakes duties involving sharps, {{org_field_name}} will provide or arrange access to sufficient information about:
- the nature and location of the work;
- the foreseeable sharps and blood-exposure risks;
- the control measures and safer-sharps devices in use;
- local induction and competency requirements;
- required PPE;
- the location of sharps containers and first-aid facilities;
- the immediate action required after an exposure;
- how to contact occupational health or another competent clinical service;
- the placement provider’s incident-reporting process; and
- the agency’s reporting and out-of-hours escalation process.
The worker must promptly inform {{org_field_name}} if the actual assignment materially differs from the information supplied, particularly where the work involves clinical procedures or sharps use that were not disclosed before placement.
10. Safe Use and Handling of Sharps
Workers must:
- avoid the use of a medical sharp where a suitable non-sharp alternative is available;
- use a safer sharp where one is provided and where its use is appropriate;
- receive instruction or demonstrate competence before using an unfamiliar safety-engineered device;
- inspect the sharp and its packaging before use;
- prepare the procedure and disposal arrangements before commencing;
- keep fingers behind the sharp point and away from the path of the instrument;
- avoid hand-to-hand passing of exposed sharps wherever reasonably practicable;
- activate the safety feature immediately after use in accordance with the manufacturer’s instructions;
- confirm, where reasonably practicable, that the safety feature has engaged;
- dispose of the sharp immediately after use;
- never leave an exposed sharp unattended; and
- report any defective or unsuitable device.
Needles must not be recapped after use. An exception may only be made where recapping is specifically required to control another identified risk, the requirement is documented in a suitable risk assessment, and a purpose-designed appliance, tool or other equipment is used so that the needle is not held directly by hand.
Workers must not:
- bend, break, remove or manipulate a used needle by hand;
- deliberately disable a safety mechanism;
- carry an exposed used sharp by hand to another room;
- place a used sharp on a tray, bed, table or other surface pending disposal;
- attempt to retrieve an item from a sharps container; or
- use improvised containers for sharps disposal.
11. Safe Disposal of Sharps
Used sharps must be disposed of immediately at the point of use into a correctly assembled, clearly marked, secure and suitable sharps container.
Workers must:
- confirm before beginning a procedure that an appropriate sharps container is available within safe reach;
- use the correct type of container for the item being disposed of;
- ensure that the container is upright, stable and positioned at a safe height;
- use the temporary closure mechanism when the container is not in active use, where applicable;
- keep containers away from children, service users and unauthorised persons;
- replace the container when it reaches the manufacturer’s fill line;
- close and secure the container in accordance with the manufacturer’s instructions and local procedure; and
- report containers that are damaged, overfilled, incorrectly assembled, poorly positioned or otherwise unsafe.
Workers must not:
- overfill a sharps container;
- force an item through the aperture;
- shake or compress the contents;
- place hands or fingers inside the container;
- remove any item from the container;
- attempt to reopen a permanently closed container; or
- dispose of sharps in ordinary domestic or clinical-waste bags.
The placement provider is responsible for arranging collection, secure storage and lawful disposal of sharps waste generated on its premises, unless a written agreement expressly allocates that responsibility differently.
12. Personal Protective Equipment
Suitable PPE must be selected on the basis of the risk assessment and the procedure being undertaken.
Depending on the task, PPE may include:
- disposable gloves;
- a fluid-resistant apron or gown;
- eye protection; and
- a face shield or fluid-resistant surgical mask where splashing to the face is foreseeable.
Gloves may reduce contamination but do not prevent a needle or other sharp from puncturing the skin. PPE must therefore be used alongside, and not as a substitute for, safer equipment, safe systems of work, suitable disposal arrangements, training and supervision.
Workers must:
- use PPE supplied for the task;
- check that it is suitable and undamaged;
- remove it safely;
- dispose of or decontaminate it in accordance with local procedure;
- perform hand hygiene after removing gloves; and
- immediately report any absence or failure of required PPE.
13. Hepatitis B Immunisation and Occupational Health
Where a risk assessment identifies foreseeable occupational exposure to blood or blood-stained body fluids, {{org_field_name}} will have arrangements to determine, through an appropriate occupational-health process, whether the worker has been offered suitable hepatitis B immunisation.
Effective immunisation must be offered to workers who are not already appropriately immunised and who are exposed to a relevant occupational risk. The vaccine must be made available without charge to the worker.
Workers must be given information about:
- the benefits and limitations of immunisation;
- the recommended vaccination course;
- post-vaccination testing where clinically indicated;
- the action required after an exposure regardless of vaccination status; and
- the confidential handling of vaccination and occupational-health information.
A worker may decline vaccination, but the decision and the information provided should be documented by the relevant occupational-health service. Refusal of vaccination does not remove the employer’s duty to control exposure by other reasonably practicable measures.
{{org_field_name}} should ordinarily receive only confirmation relevant to fitness for work, restrictions, recommended adjustments or required follow-up. Detailed clinical results must remain with the occupational-health or treating service unless disclosure is lawful and necessary.
14. Immediate Action Following a Sharps or Occupational Exposure Incident
The affected worker must stop work safely and take immediate first-aid action.
14.1 Puncture, cut or bite
The worker must:
- encourage the wound to bleed gently without squeezing or damaging the tissue;
- wash the area thoroughly with liquid soap and warm running water;
- not scrub the wound;
- not suck the wound;
- not use bleach or another caustic agent; and
- dry the area and cover it with a waterproof dressing.
14.2 Splash to the eye
The worker must:
- irrigate the eye immediately with clean running water or sterile saline;
- remove contact lenses where this can be done safely;
- avoid rubbing the eye; and
- seek urgent clinical assessment.
14.3 Splash to the mouth or nose
The worker must:
- rinse the affected area thoroughly with water;
- spit out the water used to rinse the mouth;
- not swallow the rinsing water; and
- seek urgent clinical assessment.
14.4 Contact with broken or damaged skin
The worker must wash the affected area thoroughly with soap and running water and obtain clinical advice where exposure to blood or potentially infectious material may have occurred.
14.5 Immediate notification
Following first aid, the worker must immediately:
- inform the person in charge at the placement;
- contact the placement’s occupational-health, emergency or exposure service;
- inform {{org_field_name}} through the designated telephone number;
- follow the agency’s out-of-hours procedure where the office is closed; and
- record sufficient details to support urgent clinical risk assessment.
Medical assessment must not be delayed while an internal incident form is being completed or while responsibility for the incident is being discussed.
15. Urgent Clinical Assessment and Post-Exposure Management
Every potentially significant occupational exposure must receive an urgent assessment by a suitably qualified clinician, occupational-health professional, emergency department or specialist exposure service.
The assessment should consider:
- the type and depth of injury;
- whether the sharp was used;
- the presence of visible blood;
- whether the device had been placed in a vein or artery;
- the nature and volume of the body fluid;
- the route of exposure;
- available information about the source individual;
- the worker’s hepatitis B immunisation and antibody status;
- the need for baseline blood samples;
- the need for hepatitis B vaccine or hepatitis B immunoglobulin;
- the need for HIV post-exposure prophylaxis;
- arrangements for hepatitis C testing and follow-up; and
- the worker’s pregnancy, medicines, allergies and other relevant clinical factors.
HIV post-exposure prophylaxis is time-sensitive. Where it may be clinically indicated, assessment and access to treatment must occur without delay. The decision to prescribe, amend or discontinue post-exposure medication must be made by an appropriately qualified clinician.
{{org_field_name}} must maintain a clear arrangement for obtaining urgent advice outside normal office hours. A worker must not be directed merely to wait until the agency office or routine occupational-health service reopens.
The worker must:
- follow the clinical advice provided;
- attend recommended blood tests and follow-up appointments;
- take prescribed medication as directed;
- report significant medication side-effects to the treating service; and
- seek further advice if symptoms or concerns arise.
{{org_field_name}} will provide reasonable support, including assistance with appointments, communication with the placement provider, wellbeing support and review of any work restrictions recommended by occupational health.
16. Source Individual Assessment and Testing
Where assessment or testing of the source individual may assist clinical management, it must be undertaken only by the placement provider or another authorised healthcare professional in accordance with applicable clinical, consent, confidentiality and capacity requirements.
Agency workers and agency office personnel must not:
- seek consent directly from a service user for blood-borne virus testing unless this is within their authorised professional role;
- take a source sample without proper authority and informed consent or another lawful basis;
- pressure a service user, relative or representative to agree to testing;
- access the source individual’s medical records without authorisation; or
- disclose the identity or medical information of the source individual more widely than is necessary.
A discarded sharp found in the environment must not be assumed to have been used on a particular individual unless this is reliably established.
The absence of source testing must not delay the affected worker’s urgent clinical assessment or clinically indicated treatment.
17. Internal and Statutory Incident Reporting
Every sharps injury, occupational exposure incident, defective safety device and relevant near miss must be reported promptly:
- to the placement manager or person in charge;
- through the placement provider’s incident-reporting system;
- to {{org_field_name}} through its designated reporting route; and
- to the worker’s occupational-health or treating service where clinical follow-up is required.
The report should record, so far as known:
- the date, time and location;
- the task being undertaken;
- the type of device;
- whether the device had been used;
- whether a safety feature was present and activated;
- how the incident occurred;
- the type of exposure and first aid given;
- whether urgent clinical advice was obtained;
- immediate corrective action; and
- witnesses or other relevant persons.
Confidential clinical details, source-patient information and test results must not be entered into general incident records unless they are necessary, proportionate and lawfully recorded.
17.1 RIDDOR
The organisation responsible for the work activity must determine whether the incident is reportable under the Reporting of Injuries, Diseases and Dangerous Occurrences Regulations 2013. {{org_field_name}} and the placement provider must co-operate to identify the legally responsible reporting person and must not assume that the other organisation has submitted a report.
Depending on the circumstances, reporting may be required where:
- an employee is injured by a sharp known to be contaminated with a blood-borne virus, which may constitute a dangerous occurrence;
- the worker acquires a reportable occupational infection following exposure to a biological agent;
- the incident results in death or another specified injury; or
- an injury results in the worker being unable to perform their normal work duties for more than seven consecutive days, excluding the day of the incident.
An injury resulting in more than three consecutive days’ incapacity but not more than seven days must be recorded even where it is not reportable as an over-seven-day injury.
A clean needlestick injury, or an injury from a sharp whose contamination status is unknown, is not automatically reportable solely because infection was theoretically possible. The facts must be assessed against the applicable RIDDOR category and current HSE guidance.
Any RIDDOR decision, including a decision not to report, must be documented with the reasons and the identity of the competent person who made the decision.
18. Incident Investigation and Corrective Action
{{org_field_name}} will co-operate with the placement provider to investigate sharps injuries, exposure incidents and significant near misses.
The investigation must focus on prevention and should consider:
- whether the sharp was necessary;
- whether a suitable safer sharp was available;
- whether the worker had received appropriate information, training and supervision;
- whether the worker was familiar with the device;
- whether the safety feature functioned correctly;
- whether the sharps container was suitable, correctly positioned and below the fill line;
- staffing levels, workload, fatigue, interruptions and environmental conditions;
- service-user movement or behavioural risks;
- whether PPE and first-aid arrangements were adequate;
- whether medical assessment was obtained promptly;
- whether the agency and placement provider communicated effectively; and
- whether similar incidents or warnings had previously occurred.
Corrective action may include:
- changing equipment or introducing a safer device;
- revising a risk assessment or procedure;
- relocating or replacing sharps containers;
- providing additional training or supervision;
- changing staffing arrangements;
- restricting particular duties pending competency assessment;
- escalating concerns to the placement provider’s senior management;
- suspending new placements; or
- withdrawing workers from the placement where risks are not adequately controlled.
Investigations must not automatically blame the injured worker or rely solely on retraining where equipment, workload, environment, supervision or organisational arrangements contributed to the incident.
19. Information, Instruction, Training and Competence
Workers who may be exposed to medical sharps must receive suitable information and training before undertaking relevant duties and at appropriate intervals thereafter.
Training must cover, where relevant:
- the risks of sharps injury and blood-borne virus transmission;
- applicable legal requirements;
- the hierarchy of control;
- avoidance of unnecessary sharps use;
- correct use of safer-sharps devices;
- restrictions on recapping;
- safe handling and point-of-use disposal;
- selection and use of PPE;
- hepatitis B immunisation;
- first aid after percutaneous, mucous-membrane and broken-skin exposure;
- urgent clinical assessment and post-exposure treatment;
- internal reporting, RIDDOR and investigation arrangements;
- confidentiality and the handling of health information;
- local placement procedures; and
- how to raise a safety concern or stop unsafe work.
Where practical skill is required, completion of online or classroom training alone is not sufficient. Competence must be assessed through evidence appropriate to the role, which may include supervised practice, simulation, manufacturer-specific instruction or confirmation by the placement provider.
Refresher training must be provided:
- at intervals identified by risk assessment;
- when equipment or procedures change;
- following an incident or identified competency gap;
- where monitoring shows poor compliance; and
- before a worker resumes relevant duties after a substantial period away from practice.
Training records must state the date, content, provider and assessment outcome.
20. Supervision, Welfare and Post-Incident Support
Placement providers must provide suitable local supervision having regard to the worker’s duties, experience, familiarity with the environment and the risks involved.
{{org_field_name}} will:
- ensure that workers know how to contact the agency during and outside normal office hours;
- provide confidential practical and emotional support after an incident;
- facilitate access to occupational health or another competent clinical service;
- consider temporary adjustments or restrictions recommended by a clinician;
- maintain appropriate contact during follow-up;
- avoid unnecessary disclosure of the worker’s medical information;
- provide information about employee-assistance, counselling or wellbeing services where available; and
- ensure that the worker is not pressured to continue clinical duties before urgent assessment has taken place.
A worker must not be treated adversely merely because they report an injury, seek medical advice, participate in an investigation or raise a genuine safety concern.
21. Data Protection and Confidentiality
Information about an occupational exposure, vaccination status, blood-test result, diagnosis, medication or occupational-health recommendation is health information and special-category personal data.
{{org_field_name}} will process such information in accordance with the UK GDPR and the Data Protection Act 2018, as amended by the Data (Use and Access) Act 2025.
The organisation will:
- identify and document an appropriate lawful basis and special-category condition;
- collect only information that is necessary and proportionate;
- keep clinical information separate from general placement records where practicable;
- restrict access to authorised personnel;
- use secure methods when sending information to occupational health or the placement provider;
- provide workers with relevant privacy information;
- retain information only for an identified legal, clinical or employment purpose;
- ensure that any retention period required under health and safety legislation is observed; and
- securely dispose of information when retention is no longer required.
Consent must not automatically be treated as the legal basis for routine employment-related health processing because the imbalance in the employment relationship may mean that consent is not freely given. Consent may nevertheless be relevant to specific clinical procedures or disclosure by a healthcare professional.
Managers should ordinarily receive only information about fitness for work, restrictions, adjustments and necessary follow-up, rather than detailed diagnoses or test results.
Information about a source individual must be treated as confidential and must not be disclosed to the affected worker or agency beyond what the treating clinician considers lawful and necessary for clinical management.
22. Consultation with Workers
{{org_field_name}} will consult workers, and any recognised safety representatives, on matters affecting their health and safety in accordance with applicable consultation legislation.
Consultation may include:
- selection and evaluation of safer-sharps devices where the agency has influence over equipment;
- review of training and information;
- analysis of incidents and near misses;
- placement-specific concerns;
- changes to reporting and occupational-health arrangements; and
- review of this policy.
Workers are encouraged to identify hazards and recommend improvements without fear of detriment.
23. Monitoring, Audit and Continuous Improvement
The directors and designated Health and Safety Lead will monitor:
- the number and type of sharps injuries and exposure incidents;
- near misses;
- devices or procedures repeatedly associated with incidents;
- the time between exposure and clinical assessment;
- completion of incident investigations;
- completion and effectiveness of corrective actions;
- training and competency compliance;
- placement providers’ co-operation and safety performance;
- concerns raised by workers; and
- trends indicating an increased risk at a particular placement.
Information used for management reporting should be anonymised or aggregated where individual identification is unnecessary.
Where monitoring identifies serious, repeated or unresolved shortcomings, {{org_field_name}} will consider:
- requiring an improvement plan from the placement provider;
- suspending particular duties;
- declining further bookings;
- withdrawing agency workers;
- notifying the appropriate enforcing, commissioning or regulatory body where there is a lawful and proportionate reason to do so; or
- obtaining specialist health and safety or legal advice.
24. Policy Review
This policy will be formally reviewed at least annually and sooner where:
organisational responsibilities or occupational-health arrangements change.
relevant legislation or authoritative guidance changes;
a serious sharps injury or occupational exposure occurs;
incident or near-miss trends indicate that controls may be ineffective;
new equipment or working practices are introduced;
a placement provider, worker, safety representative, occupational-health provider or enforcing authority identifies a concern;
an audit identifies non-compliance; or
Responsible Person: {{org_field_registered_manager_first_name}} {{org_field_registered_manager_last_name}}
Reviewed on: {{last_update_date}}
Next Review Date: {{next_review_date}}
Copyright © {{current_year}} – {{org_field_name}}. All rights reserved.