🏭

Manufacturing Excellence Through Compliance

Maintain ISO standards, ensure workplace safety, and optimize production quality across all facilities.

UK manufacturing contributes over £200 billion to the economy annually, yet the sector operates under one of the most demanding compliance landscapes of any industry. Factories and production facilities must simultaneously satisfy ISO 9001 quality management, ISO 14001 environmental, and ISO 45001 occupational health and safety standards, whilst meeting sector-specific obligations under PUWER, LOLER, COSHH, and — for sites handling dangerous substances above threshold quantities — the COMAH Regulations 2015. HSE manufacturing inspections routinely uncover documentation gaps, and enforcement notices can halt production lines, making proactive compliance management a business-critical discipline.

As the sector shifts toward Industry 4.0 and digital manufacturing, regulators and certification bodies alike expect compliance evidence to be digital, time-stamped, and readily available. Paper-based logbooks and spreadsheet-driven maintenance schedules are no longer adequate for demonstrating the systematic approach demanded by ISO auditors or an HSE inspector on site. Assistant Manager gives production teams, health and safety managers, and quality teams a single mobile-first platform to manage equipment inspections, COSHH assessments, shift handovers, non-conformance records, and audit documentation — ensuring that every compliance obligation is captured, evidenced, and always inspection-ready.

£224B

UK manufacturing output per year

ONS Manufacturing Statistics 2024

18,000+

Non-fatal injuries in UK manufacturing annually

HSE Manufacturing Statistics 2023/24

55%

of UK manufacturers hold ISO 9001 certification

British Standards Institution Survey 2024

3,200+

HSE inspections of manufacturing premises per year

HSE Annual Report 2023/24

Why Manufacturing Businesses Choose Us

ISO audit-ready

Reduce quality defects

Streamlined maintenance tracking

Key UK Regulations for Manufacturing

The regulations your organisation must comply with — and how Assistant Manager helps you stay on top of them.

Health and Safety at Work etc. Act 1974

c.37 Ongoing

The primary piece of health and safety legislation in Great Britain. Places a duty on employers to ensure, so far as is reasonably practicable, the health, safety, and welfare of all employees, and to conduct their undertaking in a way that does not expose non-employees to risk.

Provision and Use of Work Equipment Regulations 1998 (PUWER)

SI 1998/2306 Regular inspection; frequency risk-based

Requires that all work equipment is suitable for its intended purpose, properly maintained, and inspected at appropriate intervals. Machinery must have adequate guards, stop controls, and warning devices. Operators must be trained and authorised to use equipment.

Lifting Operations and Lifting Equipment Regulations 1998 (LOLER)

SI 1998/2307 6-monthly (equipment carrying persons); 12-monthly (other lifting equipment)

Requires lifting equipment (including cranes, hoists, fork-lift trucks, and their accessories) to be of adequate strength, marked with safe working loads, and subject to thorough examination by a competent person. Thorough examination reports must be retained.

Control of Substances Hazardous to Health Regulations 2002 (COSHH)

SI 2002/2677 Annual review; review after any significant change

Requires employers to assess the risks from substances hazardous to health (including chemicals, dust, fumes, and biological agents), implement appropriate controls, provide suitable PPE, monitor exposure where required, and provide health surveillance for at-risk employees.

Dangerous Substances and Explosive Atmospheres Regulations 2002 (DSEAR)

SI 2002/2776 Ongoing; review after process changes

Applies where flammable liquids, gases, dusts, or mists are present. Requires risk assessment of explosive atmospheres, classification of hazardous zones, prevention or control of ignition sources, and emergency procedures.

Control of Noise at Work Regulations 2005

SI 2005/1643 Noise assessment when exposure likely at or above lower action level

Sets action levels for daily and weekly noise exposure (lower: 80 dB(A); upper: 85 dB(A); limit: 87 dB(A)). Above the lower action level, employers must carry out noise risk assessments, provide hearing protection, and establish hearing protection zones.

Control of Major Accident Hazards Regulations 2015 (COMAH)

SI 2015/483 Safety report review every 5 years or after significant changes

Applies to establishments holding dangerous substances at or above threshold quantities. Lower-tier sites must notify the Competent Authority and produce a major accident prevention policy (MAPP). Upper-tier sites must also produce a safety report and on-site emergency plan.

Reporting of Injuries, Diseases and Dangerous Occurrences Regulations 2013 (RIDDOR)

SI 2013/1471 Report within 10 days (injuries); immediately (deaths and specified injuries)

Requires employers to report and keep records of work-related deaths, specified injuries, over-7-day incapacitation injuries, occupational diseases, and dangerous occurrences. Manufacturing is one of the highest-risk sectors for RIDDOR reportable incidents.

Supply of Machinery (Safety) Regulations 2008

SI 2008/1597 Pre-market; review on substantial modification

Retained EU law implementing the Machinery Directive. Requires that machinery placed on the market or put into service is safe, CE/UKCA marked, accompanied by a declaration of conformity, and supplied with adequate instructions. Relevant for manufacturers placing machinery on the UK market.

Common Manufacturing Compliance Challenges

Equipment maintenance and PUWER compliance

Manufacturing facilities typically operate hundreds of pieces of plant and machinery, each with its own inspection schedule, maintenance frequency, and operator authorisation requirements. PUWER demands that equipment is inspected at suitable intervals, with records maintained and defects actioned before the equipment is returned to use.

Uninspected or poorly maintained machinery is the leading cause of manufacturing fatalities. HSE can issue prohibition notices halting production, and employers face prosecution with unlimited fines and custodial sentences for serious breaches.

COSHH assessments for manufacturing substances

Production environments commonly involve solvents, lubricants, adhesives, cleaning agents, metal dusts, and process fumes. Each substance requires a written COSHH assessment, appropriate controls (elimination, substitution, engineering controls, PPE), and — where residual exposure risks remain — health surveillance for affected workers.

Inadequate COSHH management can cause occupational asthma, dermatitis, and long-latency conditions such as industrial deafness or respiratory disease. Enforcement action includes improvement notices, prosecution, and compensation claims from affected employees.

ISO management system documentation and audit readiness

Maintaining simultaneous certification to ISO 9001 (quality), ISO 14001 (environmental), and ISO 45001 (safety) requires a structured management system with documented procedures, calibration records, non-conformance logs, corrective action plans, and management review evidence. Auditors expect consistent implementation across all shifts and production areas.

Failed certification audits result in suspension or withdrawal of ISO certificates, which can trigger customer contract clauses, block tender opportunities, and damage competitive positioning — particularly in automotive, aerospace, and food manufacturing supply chains.

Lockout/tagout and machine guarding compliance

Isolation of energy sources (electrical, pneumatic, hydraulic, thermal) before maintenance work is a critical safe system of work in manufacturing. PUWER requires machines to have effective means of isolation, and HSE expects documented lockout/tagout (LOTO) procedures with records of every isolation. Machine guarding must be inspected regularly and any defect treated as a safety-critical issue.

Failure to isolate machinery correctly before maintenance is a primary cause of fatal accidents in manufacturing. HSE's Fatal Five in manufacturing includes contact with moving machinery, and prosecution of both the individual and the organisation is common following such incidents.

Assistant Manager addresses all these challenges with industry-specific compliance solutions.

Who It's For

Built for every role in your manufacturing organisation.

Production Manager

Responsible for day-to-day factory operations, hitting production targets, managing shift teams, and ensuring that the production floor operates safely and efficiently. Acts as first point of contact when equipment fails or a safety incident occurs.

  • Chasing paper-based equipment check sheets and shift handover records that go missing or are illegible
  • No real-time visibility of which machines have outstanding defects or overdue inspections
  • Shift handovers that fail to communicate live issues, leading to repeated problems across shifts
  • Balancing production output pressures against the time needed for thorough safety checks
  • Difficulty demonstrating to auditors and HSE inspectors that documented procedures are actually followed on the shop floor

Health & Safety Manager

Owns the factory's safety management system, conducts and reviews risk assessments, investigates incidents, liaises with the HSE, and drives a culture of continuous safety improvement across all production areas and shifts.

  • Maintaining current COSHH assessments across dozens of substances as products and processes change
  • Coordinating RIDDOR reporting accurately and on time whilst simultaneously managing the incident investigation
  • Proving to HSE inspectors that risk assessments are live documents, not filed-and-forgotten paperwork
  • Tracking corrective actions to closure after incidents or near-misses with no centralised system
  • Ensuring all shift workers, agency staff, and contractors receive and acknowledge the correct inductions and safety briefings

Quality Manager

Accountable for the factory's ISO 9001 quality management system, internal audit programme, supplier quality, non-conformance management, and customer-facing quality assurance. Manages the relationship with the certification body and coordinates management reviews.

  • Collating audit evidence from paper records and spreadsheets across multiple production lines in the run-up to a certification audit
  • Non-conformance reports (NCRs) raised but corrective actions not followed up to verified closure
  • Calibration records for measurement equipment not reliably maintained, risking audit findings
  • No single system linking quality data, non-conformances, corrective actions, and management review outputs
  • Difficulty demonstrating continuous improvement between audit cycles to satisfy ISO 9001 clause 10 requirements

Manufacturing Solutions by Sector

Explore compliance solutions tailored to your specific manufacturing sector.

How Assistant Manager Helps Manufacturing Businesses

Equipment Inspection & PUWER Compliance

Create inspection schedules for every piece of plant and machinery, with automated reminders, mobile-friendly checklists, and instant defect reporting. Every inspection is date-stamped, linked to the equipment record, and audit-ready.

COSHH Assessment Management

Store COSHH assessments digitally, link them to substances and work areas, set annual review reminders, and record employee acknowledgements. Track Safety Data Sheet versions and exposure monitoring results in one place.

ISO Audit Documentation

Maintain the documented information required by ISO 9001, 14001, and 45001 in a structured, searchable system. Generate audit evidence packs in minutes and track internal audit findings through to verified corrective action closure.

Shift Handover Checklists

Standardise shift handovers with structured digital checklists that capture live equipment issues, outstanding actions, and production notes. Ensure critical safety information is communicated consistently across every shift change.

Non-Conformance & CAPA Tracking

Raise non-conformance reports (NCRs) on mobile, assign corrective and preventive actions (CAPAs) with owners and due dates, and track resolution to verified closure. Demonstrate continuous improvement with trend analysis across production areas.

Production Safety Dashboards

Real-time visibility of compliance status across all production lines and facilities. See overdue inspections, open non-conformances, outstanding CAPAs, and incident trends at a glance — giving management the assurance that nothing is being missed.

Frequently Asked Questions

Common manufacturing compliance questions answered.

What PUWER inspections are required for manufacturing equipment?

Under PUWER 1998, the frequency and type of inspection depends on the risks associated with the equipment and the environment it operates in. There is no single prescribed interval — inspections must occur at suitable intervals, determined by a risk assessment. High-risk equipment in aggressive environments (e.g., presses, conveyors, CNC machines) typically requires more frequent checks than low-risk hand tools. Inspection records must be retained and must identify the equipment, who carried out the inspection, the date, any defects found, and action taken. Assistant Manager lets you create equipment-specific inspection schedules with automated reminders and digital records of every completed check.

How do we maintain COSHH assessments for manufacturing substances?

COSHH assessments must be documented in writing, must be suitable and sufficient, and must be reviewed when there is reason to believe they are no longer valid (e.g., after a process change, a new substance is introduced, or health surveillance reveals a problem). As a minimum, assessments should be reviewed annually. Each assessment should identify the substance, its hazardous properties (by reference to the Safety Data Sheet), who is exposed, how they are exposed, the controls in place, and any health surveillance required. Assistant Manager enables you to store assessments digitally, link them to substances and work areas, assign review dates, and record employee acknowledgements.

What are our COMAH obligations if we store dangerous substances?

If your site stores dangerous substances (including flammable liquids, toxic chemicals, or explosives) at or above the threshold quantities set out in Schedule 1 of COMAH 2015, you will be a lower-tier or upper-tier COMAH establishment. Lower-tier sites must notify the Competent Authority (HSE and Environment Agency jointly), prepare and implement a Major Accident Prevention Policy (MAPP), and review it every five years. Upper-tier sites additionally must produce a comprehensive Safety Report and on-site emergency plan, which are subject to Competent Authority assessment. Failure to comply is a criminal offence. Check the COMAH threshold quantities for your specific substances using the HSE's online tool.

How should we manage lockout/tagout (LOTO) procedures?

Lockout/tagout procedures should be documented for every machine or piece of plant that requires isolation before maintenance or cleaning. The procedure must specify every energy source (electrical, pneumatic, hydraulic, stored mechanical energy), the isolation point, the isolation device to use, and the sequence of steps. Before maintenance begins, the Permit to Work or LOTO record must be completed, signed by the authorised person, and physically attached to the isolation point. Assistant Manager can manage digital Permits to Work and LOTO authorisation records, ensuring every isolation is documented, traceable, and cannot be overlooked during shift handovers.

What noise assessments are required under the Control of Noise at Work Regulations 2005?

Employers must carry out a noise risk assessment where employees are likely to be exposed at or above the lower exposure action value of 80 dB(A) daily or weekly average. The assessment must identify who is at risk, estimate exposures, identify controls already in place, and determine whether further action is needed. Above the upper action value of 85 dB(A), employers must introduce technical and organisational controls to reduce noise, provide and ensure the use of hearing protection, and establish hearing protection zones. Health surveillance (audiometry) is required for employees regularly exposed at or above the upper action value. Assessments should be reviewed when working conditions change significantly.

How do we prepare for an HSE manufacturing inspection?

HSE manufacturing inspectors typically examine whether your health and safety management system is effectively implemented, not just documented. Key areas include: written risk assessments that reflect actual working conditions; evidence that PUWER and LOLER inspection schedules are up to date; COSHH assessments and monitoring records for significant substances; accident and near-miss records with completed investigations; training records for all employees including machinery operators; and evidence that corrective actions from previous inspections or incidents have been completed. Assistant Manager provides a real-time compliance dashboard showing overdue inspections, outstanding actions, and any gaps — giving you the assurance that you are always ready for an unannounced visit.

What records are needed for ISO 9001 compliance?

ISO 9001:2015 requires organisations to maintain documented information (records) to provide evidence that its processes are being carried out as planned. Key mandatory records include: calibration records for monitoring and measuring equipment; records of competence and training; non-conformance records and the results of corrective actions; results of management reviews; internal audit programme and results; and evidence of customer communication and satisfaction. Beyond the mandatory minimum, most manufacturers also retain production records, inspection and test records, supplier evaluation records, and change control records. All records must be legible, identifiable, and retrievable. Assistant Manager structures these records digitally with search, filter, and export capabilities for audit preparation.

How should we document and investigate manufacturing incidents under RIDDOR?

When a RIDDOR-reportable incident occurs, you must report it to the HSE promptly (immediately for deaths and specified injuries; within 10 days for over-7-day injuries; within 15 days for occupational diseases). You must also keep a record of the incident for at least three years. Separately — and regardless of whether RIDDOR applies — a thorough internal investigation should document the sequence of events, immediate and root causes, contributing factors, and corrective actions. Investigation records are essential evidence that you have taken the incident seriously and implemented controls to prevent recurrence, which HSE inspectors will want to review. Assistant Manager provides structured incident report forms, investigation workflows, and action tracking to closure, with automated prompts for RIDDOR reportable thresholds.

Ready to Transform Your Manufacturing Compliance?

Join thousands of manufacturing businesses already using Assistant Manager to simplify compliance and reduce risk.

Copyright © 2026 Assistant Manager. All rights reserved.