{"title":"Featured toolkits","description":"\u003cp\u003eA rotating selection of the standards teams ask us for most often.\u003c\/p\u003e","products":[{"product_id":"brcgs-global-standard-food-safety-issue-9","title":"BRCGS Global Standard Food Safety, Issue 9","description":"\u003cp\u003e\u003cem\u003eA complete BRCGS Issue 9 food safety and quality system, mapped clause by clause so your site evidences conformity in the auditor's own language.\u003c\/em\u003e\u003c\/p\u003e\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eThe \u003cstrong\u003eBRCGS Global Standard for Food Safety, Issue 9\u003c\/strong\u003e is a GFSI-benchmarked scheme covering the safety, legality and quality of food from manufacturers and processors in every product category, and required by retailers and brand owners across the UK, Europe and beyond. This system builds what the Standard assumes is already running: senior management commitment, a documented HACCP plan aligned with Codex Alimentarius principles, and the quality management system underpinning both.\u003c\/p\u003e\n\u003cp\u003eRequirements split into fundamental clauses, where non-conformity can prevent certification, and detailed sections on site standards, product control, process control and personnel, including high-risk, high-care and ambient high-care production zones. Issue 9 presses harder on food safety culture, product authenticity and food fraud defence, and environmental monitoring, while keeping the AA+ to D grading scale and the announced or unannounced audit options. Certification comes from a body accredited to ISO\/IEC 17065, valid twelve months on an annual re-audit cycle.\u003c\/p\u003e\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eHACCP from prerequisite programmes and hazard identification to CCP corrective action, verification and validation.\u003c\/li\u003e\n\u003cli\u003eSite standards and hygiene: pre-operational inspection, sanitation limits, glass and brittle plastic control, PPE discipline.\u003c\/li\u003e\n\u003cli\u003eAllergen management and product authenticity, covering additives, acrylamide, heavy metals, mycotoxins and irradiation.\u003c\/li\u003e\n\u003cli\u003eProcess control and equipment integrity: metal detector verification, preventive maintenance, calibration of measuring devices.\u003c\/li\u003e\n\u003cli\u003eTraceability, product withdrawal and recall, emergency preparedness, and reliability of laboratory test results.\u003c\/li\u003e\n\u003cli\u003eFood safety culture as a managed programme, with site security and food defence assessment.\u003c\/li\u003e\n\u003cli\u003eGovernance: document control, internal audit, management review, corrective action, non-conforming product.\u003c\/li\u003e\n\u003cli\u003eDepartmental process mapping and training in hygiene, HACCP awareness, allergens and foreign-body control.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eQA and technical managers, food safety team leaders and the consultants supporting them at manufacturing sites facing a first BRCGS audit, an Issue 9 transition, or a retailer listing conditional on a GFSI-recognised certificate. You edit it to match your products, process zones and equipment, and reach the audit with documentation that traces to the clause each part answers.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517049745748,"sku":"AGS-01-001","price":690.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/AGS-01-001_BRCGS_Issue_9.png?v=1787339147"},{"product_id":"fssc-22000-v6-management-system","title":"FSSC-22000 v6 Management System","description":"\u003cp\u003e\u003cem\u003eISO 22000, the sector prerequisite programmes and the FSSC additional requirements in one version 6 system.\u003c\/em\u003e\u003c\/p\u003e\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eFSSC 22000 version 6 is a GFSI-recognised food safety certification scheme built on ISO 22000, sector-specific prerequisite programme requirements and a defined set of additional FSSC requirements. It is used in food and feed manufacturing, food packaging production, catering, retail, and transport and storage, with certification scope fixed by the relevant food chain category. The documentation keeps that three-part construction: the ISO 22000 clauses, the prerequisite programme specification from the ISO\/TS 22002 series or its equivalent, and each additional requirement.\u003c\/p\u003e\n\u003cp\u003eISO 22000 supplies the High-Level Structure, the Plan-Do-Check-Act cycle, risk-based thinking at organisational and operational level, and prerequisite programmes combined with HACCP principles. The additional requirements sit on top, and version 6 tightens alignment with the updated ISO 22000 while raising expectations on food safety culture, quality, equipment management and environmental sustainability in line with GFSI benchmarking. Certification runs through accredited certification bodies: a two-stage initial audit, annual surveillance and periodic recertification on a three-year cycle, with provision for unannounced audits.\u003c\/p\u003e\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eThe FSSC additional requirements: services, labelling, food defence, food fraud, allergens, environmental monitoring, equipment, food loss and waste\u003c\/li\u003e\n\u003cli\u003eFood safety and quality culture, with scheme logo and claims use\u003c\/li\u003e\n\u003cli\u003eHazard control: preliminary analysis, prerequisite programmes, hazard identification and the HACCP plan\u003c\/li\u003e\n\u003cli\u003ePrerequisite programmes to ISO\/TS 22002-1, checked against the specification and by site inspection\u003c\/li\u003e\n\u003cli\u003ePurchasing and supplier control: incoming inspection, approved vendors and supplier audit scheduling\u003c\/li\u003e\n\u003cli\u003eEquipment and infrastructure: preventive maintenance, breakdown history and building fabric\u003c\/li\u003e\n\u003cli\u003eProduct design and development, production planning and disposal of non-conforming product\u003c\/li\u003e\n\u003cli\u003eDocumented information: master lists, record retention and a version 6 requirement map\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eFood and feed manufacturers, packaging producers and food chain operators whose customers require GFSI recognition, and quality managers already certified who are working through the move to version 6. The purchase point is a stage 1 audit date, a transition deadline, or the discovery that the additional requirements have no documented home. The end state is ISO structure, prerequisite programmes referenced to the technical specification, and every additional requirement traceable when an unannounced auditor asks.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517051416916,"sku":"AGS-01-005","price":490.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/AGS-01-005_FSSC_22000_v6.png?v=1787339147"},{"product_id":"haccp-hotels-management-system","title":"HACCP Hotels Management System","description":"\u003cp\u003e\u003cem\u003eRestaurants, banqueting, room service, bars and staff dining sit under one roof and one reputation, and this system holds them to a single standard.\u003c\/em\u003e\u003c\/p\u003e\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eA hotel runs several food businesses at once. Restaurant kitchens, banqueting at volume, a buffet on open display, room service, bars, minibar stock and a staff dining room each work to their own rhythm, yet share one general manager and one online reputation. This HACCP-based system is written to harmonise them, so a control that holds in the main kitchen holds equally on the banquet floor.\u003c\/p\u003e\n\u003cp\u003eBuilt on the Codex Alimentarius seven principles and twelve steps, it covers prerequisite programmes, full hazard analysis, CCP identification, critical limits, monitoring, corrective action, verification and record-keeping, through a hotel HACCP plan and study written for multi-outlet, multi-cuisine operations. The hotel food safety manual carries group policy and the HACCP team; procedures and forms enforce consistent temperature control, allergen management and CCP monitoring across outlets; checklists convert the plan into daily routines at each kitchen and service point. Induction and training material is pitched for a large, multilingual workforce, because a brand auditor asks for evidence of competence after the records.\u003c\/p\u003e\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eBuffet and banquet service — set-up, display and holding temperatures, replenishment and protection of open food.\u003c\/li\u003e\n\u003cli\u003eRoom service and in-room dining, with trolley and delivery checks for food that travels the property.\u003c\/li\u003e\n\u003cli\u003eCooking, cooling and reheating under cook, hold, chill and reheat guidance, with daily CCP monitoring and allergen management across multi-cuisine kitchens.\u003c\/li\u003e\n\u003cli\u003eGoods receiving, storage and cold chain logging, with supplier approval and purchasing control.\u003c\/li\u003e\n\u003cli\u003eGlass and brittle-plastic control in bars and service areas, alongside cleaning, sanitation and pest control.\u003c\/li\u003e\n\u003cli\u003eOutlet opening and closing, site hygiene and GMP inspection, internal audit, traceability and recall.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eFood and beverage directors, executive chefs and hygiene managers in hotels and resorts facing a brand-standard or franchise requirement, tour-operator and corporate-client due diligence, a municipal inspection, or a certification project. Edit the outlets, menus and service styles into the plan, and the property gains one framework, the same CCP evidence from banqueting to room service, and the training records beside it.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517052629332,"sku":"AGS-01-015","price":390.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/HACCP-Hotels-Management-System.png?v=1784574577"},{"product_id":"ems-iso14001-2026","title":"EMS ISO14001-2026","description":"\u003cp\u003e\u003cem\u003eAn environmental management system documented clause by clause, from significant aspects through to management review.\u003c\/em\u003e\u003c\/p\u003e\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eISO 14001 is the most widely adopted standard for environmental management systems, published by the International Organization for Standardization and used by manufacturers, service providers and public bodies of any size or sector. This system follows the standard's Annex SL high-level structure — context of the organisation, leadership, planning, support, operation, performance evaluation and improvement — so each element sits where an auditor expects to find it. The Plan-Do-Check-Act cycle runs through the whole set, and the internal audit tool is written against the ISO 14001:2026 edition.\u003c\/p\u003e\n\u003cp\u003eIts technical core is the evaluation of environmental aspects and impacts with a life-cycle perspective, with guidance on how significance is scored and a register carrying the result. It then works through compliance obligations and their periodic evaluation, environmental objectives and programmes, operational planning and control, emergency preparedness with test records, monitoring and measurement, internal audit, management review and corrective action. Because ISO 14001 shares its structure with ISO 9001 and ISO 50001, the set can be merged into an integrated management system, and its outputs feed the United Nations Sustainable Development Goals and corporate ESG reporting.\u003c\/p\u003e\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eEnvironmental aspects and impacts — identification, significance evaluation and the life-cycle perspective behind the register\u003c\/li\u003e\n\u003cli\u003eCompliance obligations — capturing legal and other requirements, then evaluating compliance on a defined cycle\u003c\/li\u003e\n\u003cli\u003eObjectives and operational control — targets, programmes, waste streams and the day-to-day controls holding them\u003c\/li\u003e\n\u003cli\u003eEmergency preparedness and response — scenarios, response arrangements, drills and inspection records\u003c\/li\u003e\n\u003cli\u003eMonitoring and measurement — what is measured, by whom, and against which criteria\u003c\/li\u003e\n\u003cli\u003eInternal audit and management review — audit programme, clause-level coverage and structured review inputs\u003c\/li\u003e\n\u003cli\u003eNonconformity and corrective action — root cause analysis, correction and continual improvement\u003c\/li\u003e\n\u003cli\u003eCompetence, communication and documented information — training, awareness, change control and records\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eEnvironmental and HSE managers, quality managers and consultants preparing for a stage 1 and stage 2 certification audit, a recertification cycle, or a customer requirement to hold ISO 14001. It suits sites already running ISO 9001 that want the environmental system on the same document control and audit rhythm. Once the aspects register, compliance obligations, objectives and audit evidence carry your own operations, the organisation can meet an accredited certification body with a system that is complete and demonstrably in use.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517059543380,"sku":"AGS-04-001","price":790.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/EMS-ISO14001-2026.png?v=1784574605"},{"product_id":"isms-iso27001-2022","title":"ISMS - ISO\/IEC 27001:2022","description":"\u003cp\u003e\u003cem\u003eA documented ISO\/IEC 27001:2022 information security management system, from the risk method through to a defensible Statement of Applicability.\u003c\/em\u003e\u003c\/p\u003e\n\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eISO\/IEC 27001:2022 specifies the requirements for establishing, implementing, maintaining and continually improving an information security management system, protecting the confidentiality, integrity and availability of information through a systematic, risk-based approach. It applies to any organisation regardless of size, sector or geography, and speaks to management, security professionals, auditors and anyone accountable for governing information risk. The clauses follow the Annex SL structure, from organisational context and leadership through planning, support, operation and performance evaluation to improvement, with Plan-Do-Check-Act embedded throughout.\u003c\/p\u003e\n\u003cp\u003eRisk assessment and treatment sits at the centre, supported by a Statement of Applicability that justifies the selection or exclusion of each control. Annex A of the 2022 revision organises its controls into organisational, people, physical and technological themes, aligned to the implementation guidance in ISO\/IEC 27002:2022. The shared Annex SL basis makes integration with ISO\/IEC 20000-1, ISO 9001 and ISO\/IEC 42001 straightforward, and the system sits alongside ISO\/IEC 27005 for risk, ISO\/IEC 27017 for cloud services and ISO\/IEC 27701 for privacy.\u003c\/p\u003e\n\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eContext, scope and interested parties: fixing ISMS boundaries and the issues behind them\u003c\/li\u003e\n\u003cli\u003eRisk assessment and treatment: criteria, risk ownership and acceptance of residual risk\u003c\/li\u003e\n\u003cli\u003eStatement of Applicability: justifying every Annex A control applied or excluded\u003c\/li\u003e\n\u003cli\u003eAccess control and identity management: provisioning, privileged access and periodic review\u003c\/li\u003e\n\u003cli\u003eAsset management and classification: inventory, ownership, handling rules and retention\u003c\/li\u003e\n\u003cli\u003eInformation security incident management: detection, reporting, escalation and corrective action\u003c\/li\u003e\n\u003cli\u003eBusiness continuity, ICT readiness and operations security\u003c\/li\u003e\n\u003cli\u003eSupplier and third-party security: evaluation, contractual requirements and ongoing assurance\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eWritten for the information security manager, IT lead or compliance officer handed a certification deadline, a client security questionnaire or a tender naming ISO\/IEC 27001. It supplies the manual, procedures, registers and audit tools an assessor expects to see, \u003cstrong\u003eready to be scoped to your organisation and populated with real evidence\u003c\/strong\u003e.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517061902676,"sku":"AGS-06-001","price":790.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/ISMS-ISO27001-2022.png?v=1784574577"},{"product_id":"iso-iec-17025-management-system","title":"ISO\/IEC 17025:2017 Management System","description":"\u003cp\u003e\u003cem\u003eEvery result your laboratory releases has to hold up in front of the customer, the regulator and the accreditation assessor.\u003c\/em\u003e\u003c\/p\u003e\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003eA laboratory is accredited on three words — competence, impartiality and consistency — and ISO\/IEC 17025:2017 is where they are given operational meaning. It applies to any organisation performing laboratory activities, whatever its size or scope, including laboratories inside a larger parent. Its requirements fall into general, structural, resource and process groups: impartiality and confidentiality; organisation and responsibilities; personnel, facilities, equipment, metrological traceability and external providers; then method selection and validation, sampling, measurement uncertainty, validity of results, reporting and nonconforming work. This system follows that structure.\u003c\/p\u003e\u003cp\u003eThe technical weight sits where assessors concentrate. Measurement uncertainty is evaluated on calculation sheets and stated on reports; metrological traceability is established and defended; calibration periodicity is scheduled and supported by intermediate checks between calibrations; and decision rules govern any statement of conformity placed against a specification. Test request and sampling sheets are drafted for water and waste water, process stack, ambient air, noise and sludge, and a schedule of activities defines the scope of accreditation claimed. The management system may follow the prescriptive route or align with ISO 9001, and accreditation bodies operating under ISO\/IEC 17011, generally within the ILAC arrangement, assess against it.\u003c\/p\u003e\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eMeasurement uncertainty — evaluation, calculation and how uncertainty is expressed on a report\u003c\/li\u003e\n\u003cli\u003eMetrological traceability and calibration — calibration periodicity, intermediate checks and equipment history\u003c\/li\u003e\n\u003cli\u003eMethod verification and validation, and the controlled introduction of a new method\u003c\/li\u003e\n\u003cli\u003eDecision rules and statements of conformity against a specification\u003c\/li\u003e\n\u003cli\u003eSampling and item handling — sheets for water, waste water, stack, ambient air, noise and sludge, plus receipt, storage and item integrity\u003c\/li\u003e\n\u003cli\u003eValidity of results — internal quality checks against defined acceptance criteria, and control of nonconforming work\u003c\/li\u003e\n\u003cli\u003eImpartiality, confidentiality, laboratory environmental conditions and verification of reports before release\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eWho it's for\u003c\/h2\u003e\u003cp\u003eAimed at the quality or technical manager of a testing or calibration laboratory — environmental testing laboratories in particular, given the sampling coverage — facing a first accreditation assessment, a reassessment or an extension of scope onto new methods. The result is a laboratory whose uncertainty budgets, traceability chain, method validation records and pre-release report checks live in one coherent set instead of being reassembled whenever an assessor is booked.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517062721876,"sku":"AGS-07-002","price":1290.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/ISO-IEC-17025-Management-System.png?v=1784574577"},{"product_id":"iso-22301-2019-business-continuity-management-system","title":"ISO 22301-2019-Business Continuity Management System","description":"\u003cp\u003e\u003cem\u003ePlan for the disruption before it arrives, and show afterwards that the plan was exercised.\u003c\/em\u003e\u003c\/p\u003e\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eISO 22301:2019 specifies requirements for a business continuity management system (BCMS) — the arrangements that let an organisation prepare for, respond to and recover from disruptive incidents while critical activities keep running at predefined acceptable levels. Natural disasters, cyber-attacks, supply chain failure, pandemics and technology outages all sit inside that scope. The set follows the standard's own sequence under the ISO harmonised high-level structure (Annex SL) and the Plan-Do-Check-Act cycle.\u003c\/p\u003e\n\u003cp\u003eThe operational weight sits in the business impact analysis and the continuity risk assessment, which establish what is critical, what it depends on, and the recovery time objective, recovery point objective and maximum tolerable period of disruption that govern the response. Strategy selection follows, then continuity plans, an incident response structure and warning arrangements; exercising, internal audit and management review close the cycle. Sharing Annex SL, ISO 22301 integrates with ISO 9001, ISO 27001 and ISO 31000, with implementation guidance in ISO 22313. Gap analysis and audit material are included for organisations working towards accredited third-party certification.\u003c\/p\u003e\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eBusiness impact analysis — critical activities, dependencies, RTO, RPO and maximum tolerable period of disruption\u003c\/li\u003e\n\u003cli\u003eContinuity risk assessment — threat scenarios, single points of failure and proportionate treatment\u003c\/li\u003e\n\u003cli\u003eContinuity strategy — people, premises, technology and supplier options against minimum acceptable service levels\u003c\/li\u003e\n\u003cli\u003ePlans and response structure — activation criteria, incident roles, escalation and stand-down\u003c\/li\u003e\n\u003cli\u003eWarning and communication — alerting staff, customers, suppliers and regulators during an incident\u003c\/li\u003e\n\u003cli\u003eExercise and testing — desktop, walkthrough and live exercises, with reporting and follow-up\u003c\/li\u003e\n\u003cli\u003ePerformance evaluation — monitoring, internal audit and management review of the defined scope\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eBusiness continuity and risk managers, operations directors and quality leads in organisations of any size, public, private or not-for-profit, who have been asked for a management system rather than a folder of recovery notes. The trigger is usually a certification decision, a customer contract, a regulator's expectations, or an incident that exposed how little was written down. You end with a defined scope, a completed impact analysis, exercised plans and an evidence trail an auditor can follow.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517064655188,"sku":"AGS-08-001","price":790.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/ISO-22301-2019-Business-Continuity-Management-System.png?v=1784574577"},{"product_id":"iso-13485-2016-medical-qms","title":"ISO 13485-2016-Medical QMS","description":"\u003cp\u003e\u003cem\u003eDesign input through to post-market feedback, held in one medical device quality system.\u003c\/em\u003e\u003c\/p\u003e\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eISO 13485:2016 sets out the requirements for a quality management system covering the design, development, production, installation and servicing of medical devices and related services. It is used by device manufacturers, suppliers of components and materials, sterilisation providers and distributors, whatever their size or type, and every requirement bends towards one end: that devices consistently meet customer and applicable regulatory requirements, with patient safety and product effectiveness as the overriding emphasis.\u003c\/p\u003e\n\u003cp\u003eBuilt on the ISO 9001 process approach, ISO 13485 presses harder on regulatory compliance, on risk management applied throughout product realisation, and on keeping processes documented. Its requirements run through management responsibility and a documented QMS; design and development controls and the medical device file; document and record control; risk management aligned with ISO 14971 principles; control of production and service provision, including cleanliness, contamination control and sterilisation where applicable; validation of processes and software; identification and traceability of devices; and complaints, adverse-event reporting, corrective and preventive action and post-market feedback. It sits beneath the frameworks that decide market access — the EU Medical Device Regulation, the FDA Quality System Regulation and the requirements underpinning the Medical Device Single Audit Program — and certification is granted by an accredited body after audit, then held through surveillance and recertification.\u003c\/p\u003e\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eDesign and development control — design plan, design review, verification and validation, and the device file\u003c\/li\u003e\n\u003cli\u003eHazard analysis and risk management through product realisation on ISO 14971 principles\u003c\/li\u003e\n\u003cli\u003eSterilisation and cleanliness — sterilisation process validation, biological indicator checks and temperature records\u003c\/li\u003e\n\u003cli\u003eProduction, engineering, stores, installation and servicing, each defined as a controlled process\u003c\/li\u003e\n\u003cli\u003eIdentification and traceability of devices, with control and disposal of non-conforming product\u003c\/li\u003e\n\u003cli\u003eCustomer feedback, complaints, medical practitioner feedback and corrective and preventive action\u003c\/li\u003e\n\u003cli\u003ePurchasing and supplier control, preventive maintenance and breakdown history\u003c\/li\u003e\n\u003cli\u003eInternal audit by clause and by department, competency matrices and management review\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eRegulatory affairs and quality managers at device manufacturers, contract producers and component suppliers needing a certifiable system standing up before a notified body assessment, an MDSAP audit or a customer's regulatory due diligence. They end with design controls, risk files and post-market processes written down and cross-referenced, ready for their own device data and process limits.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517065605460,"sku":"AGS-09-004","price":1900.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/ISO-13485-2016-Medical-QMS.png?v=1784574573"},{"product_id":"jci-hospitals-qms","title":"JCI - Hospitals (QMS), 8th Edition 2025","description":"\u003cp\u003e\u003cem\u003eA complete hospital quality management system aligned to the JCI 8th Edition — one documented management-system package for every applicable chapter, from the International Patient Safety Goals to Global Health Impact.\u003c\/em\u003e\u003c\/p\u003e\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eThe Joint Commission International Accreditation Standards for Hospitals, 8th Edition (2025) assess a hospital through four applicable sections: Accreditation Participation Requirements, Patient-Centered Care, Health Care Organization Management and Global Health Impact. Surveyors work by tracer methodology — following real patients, medications and staff files through the organisation — and expect every chapter to stand on approved policy, working procedures and completed records rather than intentions.\u003c\/p\u003e\n\u003cp\u003eThis system documents that architecture chapter by chapter. Each of the sixteen applicable chapters — APR, IPSG, ACC, AOP, ASC, COP, MMU, PCC, FMS, GLD, HCT, MOI, PCI, QPS, SQE and GHI — arrives as its own management-system package. A generated master index sits at the repository root as the front door, the controlled document register under MOI carries version and approval authority, and the Academic Medical Center chapters (MPE, HRP) are handled through a documented applicability decision rather than silently omitted.\u003c\/p\u003e\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cp\u003eThe folder architecture mirrors the standards’ own order, so a surveyor, consultant or department head can navigate it without translation. Every chapter package follows the same controlled layout:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eQuality Manual and policy — the chapter’s apex documents\u003c\/li\u003e\n\u003cli\u003eScheme — the chapter’s system map and its own document list\u003c\/li\u003e\n\u003cli\u003eProcedures, forms, and the registers and logs that evidence conformity\u003c\/li\u003e\n\u003cli\u003eChecklists, including a JCI tracer self-assessment for survey rehearsal\u003c\/li\u003e\n\u003cli\u003eGuidance and training — implementation notes, survey-readiness material and competency records\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eOwnership is assigned the way hospitals actually run: medication management to the chief pharmacist, facility safety to the facilities director, staff qualifications to human resources, with the quality director holding APR, IPSG and QPS. A master implementation roadmap in APR sequences the build from first gap assessment to survey week.\u003c\/p\u003e\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eHospitals preparing for a first JCI survey or re-accreditation under the 8th Edition, quality and accreditation directors who own the documentation burden, department leaders who must bring their chapter to survey-readiness, and consultancies running JCI programmes across client hospitals.\u003c\/p\u003e\n\u003cp\u003e\u003cem\u003eAGS is an independent publisher. References to Joint Commission International (JCI) are for identification only; this documentation is aligned to the published standards and is not issued, endorsed by, or affiliated with JCI, and does not guarantee accreditation.\u003c\/em\u003e\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56517075042644,"sku":"AGS-11-019","price":2490.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/AGS-11-019.png?v=1788399603"},{"product_id":"occupational-health-safety-management-system-iso-45001","title":"Occupational Health \u0026 Safety Management System (ISO 45001)","description":"\u003cp\u003e\u003cem\u003eA clause-by-clause health and safety system in the UAE national adoption of ISO 45001, ordered the way an auditor works through the standard.\u003c\/em\u003e\u003c\/p\u003e\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003eThe system is built on UAE.S ISO 45001:2019, and its procedures run through Clauses 4 to 10 in sequence, so the standard and the documentation can be read side by side during an audit. The OHS Management System Manual and OHS Policy arrive with document control, approval, revision history and a controlled distribution list already structured. The Management System Scheme holds the architecture, PDCA model, process map, organisation chart and a clause-to-document matrix that answers the auditor's question with a document code, and a read-me-first index sets a deployment order for organisations starting from nothing.\u003c\/p\u003e\u003cp\u003eBelow that framework sits the substance of occupational health and safety rather than only its paperwork: hazard identification and risk assessment, legal and other requirements, worker consultation and participation, operational control and permit to work, management of change, procurement and contractor management, emergency preparedness and response, incident reporting and investigation, and performance evaluation. The checklists work at site level rather than clause level, covering workplace safety inspection, work at height with ladders and scaffolds, vehicle and driving safety, fire safety equipment, and first aid and welfare facilities.\u003c\/p\u003e\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eHazard identification and risk assessment — HIRA method and register, with a review checklist testing the assessments themselves\u003c\/li\u003e\n\u003cli\u003eOperational control and permit to work — permits for higher-risk activity, with management of change alongside\u003c\/li\u003e\n\u003cli\u003eWorker consultation and participation — communication, consultation and toolbox talk records\u003c\/li\u003e\n\u003cli\u003eProcurement and contractor management — contractor HSE evaluation before award and monitoring on site\u003c\/li\u003e\n\u003cli\u003eEmergency preparedness and response — drill reports, fire safety equipment, first aid and welfare facilities\u003c\/li\u003e\n\u003cli\u003eIncident reporting and investigation — investigation, root cause, corrective action and closure\u003c\/li\u003e\n\u003cli\u003eLegal compliance and performance evaluation — legal register and evaluation, the OHS dashboard, internal audit and management review\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eWho it's for\u003c\/h2\u003e\u003cp\u003eUAE organisations pursuing ISO 45001 certification in construction, manufacturing, facilities management, logistics, hospitality and services, along with the HSE managers and officers who own the system and the consultancies that implement it. The usual trigger is a certification audit date or a client prequalification demanding a certified safety system. What follows is documentation that maps to the standard clause by clause, and checklists a supervisor can take onto site the same week.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":56792715755860,"sku":"AGS-07-027","price":790.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/AGS-07-027_ISO45001_OHS_MS.png?v=1786639546"},{"product_id":"saudi-pdpl-compliance-management-system","title":"Saudi PDPL Compliance Management System","description":"\u003cp\u003e\u003cem\u003eA documented Saudi PDPL compliance management system, from gap assessment and records of processing through to breach response and defensible destruction records.\u003c\/em\u003e\u003c\/p\u003e\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eThe Saudi Personal Data Protection Law (PDPL) — Royal Decree M\/19 of 9\/2\/1443H, as amended by Royal Decree M\/148 of 5\/9\/1444H — governs how the personal data of individuals in the Kingdom is collected, processed, disclosed and transferred. Together with its Implementing Regulation and the Regulation on Personal Data Transfer outside the Kingdom, and under the supervision of the Saudi Data \u0026amp; AI Authority (SDAIA), it imposes concrete duties: lawful bases and consent management, privacy notices, data subject rights handling, records of processing activities, controller–processor arrangements, transfer assessments, breach notification and secure destruction.\u003c\/p\u003e\n\u003cp\u003eMeeting those duties is a documentation exercise as much as a legal one. Regulators, auditors and counterparties expect approved policies, working procedures, completed registers and an evidence trail — not a legal memo. This system provides that documented layer: a controlled set of Word and Excel documents built on the official Saudi sources, with every requirement tagged to distinguish legal obligations under the PDPL and its regulations from organisational controls and recommended practice.\u003c\/p\u003e\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cp\u003eThe system is organised as a working management loop. An apex compliance manual sets the framework; policies and procedures sit with their operational domains — privacy governance and the DPO role, data subject rights, consent, data sharing and disclosure, processor management, international transfers, retention and destruction, and data security and breach management. Fillable forms, Excel registers and checklists turn each procedure into evidence, and a regulatory compliance matrix maps PDPL Articles 1–43 and Implementing Regulation Articles 1–38 to the documents that satisfy them.\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eGap assessment methodology and checklists to baseline your current position\u003c\/li\u003e\n\u003cli\u003eROPA management and a ready-to-populate register of processing activities\u003c\/li\u003e\n\u003cli\u003eDPIA screening, international transfer assessments and processor due diligence\u003c\/li\u003e\n\u003cli\u003eBreach assessment and response procedures with notification content templates\u003c\/li\u003e\n\u003cli\u003eInternal audit, corrective action, management review and a full training pack\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eBuilt for data protection officers, privacy and compliance managers, and legal counsel in organisations operating in Saudi Arabia — and for international groups whose processing of Saudi personal data brings them within the PDPL's scope. It suits banks, insurers, healthcare providers, retailers and technology companies alike, and gives consultancies a consistent, source-traceable foundation for delivering PDPL programmes across clients.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":57017074418004,"sku":"AGS-19-001","price":1950.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/AGS-19-001.png?v=1788398406"},{"product_id":"dora-ict-third-party-risk-digital-operational-resilience-management-system","title":"DORA ICT Third-Party Risk \u0026 Digital Operational Resilience Management System","description":"\u003cp\u003e\u003cem\u003eA documented DORA management system under Regulation (EU) 2022\/2554 — from ICT risk governance and major-incident reporting to the Register of Information, threat-led penetration testing and a defensible exit strategy for every critical provider.\u003c\/em\u003e\u003c\/p\u003e\n\u003ch2\u003eOverview\u003c\/h2\u003e\n\u003cp\u003eThe Digital Operational Resilience Act — Regulation (EU) 2022\/2554 — has applied to financial entities across the EU since 17 January 2025. It replaces fragmented ICT guidance with a single supervisory regime spanning ICT risk management, incident classification and reporting, digital operational resilience testing, ICT third-party risk and information sharing. Responsibility sits explicitly with the management body, and supervisors expect a documented, evidenced framework rather than a collection of ad hoc controls.\u003c\/p\u003e\n\u003cp\u003eThis toolkit documents that framework end to end. It is built against DORA and its Level-2 measures — Commission Delegated Regulations (EU) 2024\/1772 on incident classification, 2024\/1773 on the third-party policy and 2024\/1774 on the ICT risk management framework, and Implementing Regulation (EU) 2024\/2956 on the Register of Information — with a regulatory version-control register and change log that track the 2025 acts on incident reporting ((EU) 2025\/301 and 2025\/302), subcontracting ((EU) 2025\/532) and TLPT ((EU) 2025\/1190), so each is confirmed against the Official Journal before the dependent controls are relied upon.\u003c\/p\u003e\n\u003ch2\u003eWhat this system covers\u003c\/h2\u003e\n\u003cp\u003eA management manual anchors the system; policies and procedures then work through each obligation in operating detail, supported by forms, checklists and Excel registers, calculators and dashboards that become your live compliance records. A requirements traceability matrix maps the documentation back to the regulation, and a seventeen-phase implementation roadmap, guidance library and training modules take the team from the initial applicability assessment through to management review and internal audit. The modules cover:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eICT risk management — asset inventory, dependency mapping and critical or important function identification\u003c\/li\u003e\n\u003cli\u003eIncident management — classification, significant cyber threat assessment and major-incident reporting\u003c\/li\u003e\n\u003cli\u003eResilience testing and TLPT governance\u003c\/li\u003e\n\u003cli\u003eThe full third-party lifecycle — due diligence, contractual compliance, subcontracting and fourth-party risk, concentration risk, monitoring and exit\u003c\/li\u003e\n\u003cli\u003eThe Register of Information, with data-quality validation\u003c\/li\u003e\n\u003cli\u003eDigital operational resilience — business impact analysis, impact tolerances, continuity, disaster recovery, crisis management and a severe-but-plausible scenario library\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003eWho it's for\u003c\/h2\u003e\n\u003cp\u003eHeads of ICT risk and operational resilience, DORA compliance officers, CISOs and third-party risk managers at banks, insurers, investment firms, payment and e-money institutions and crypto-asset service providers within the scope of DORA — and the consultancies building DORA programmes for them. It suits entities documenting the regime for the first time as well as those consolidating scattered artefacts into one traceable system ahead of a supervisory review.\u003c\/p\u003e","brand":"Apex Global Solutions AGS","offers":[{"title":"Default Title","offer_id":57017075269972,"sku":"AGS-20-001","price":2450.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1052\/4996\/4372\/files\/AGS-20-001.png?v=1788398420"}],"url":"https:\/\/agskits.com\/collections\/featured-toolkits.oembed","provider":"Apex Global Solutions","version":"1.0","type":"link"}