Are checklist PDFs controlled quality records?
No. They are preparation tools until adopted inside the organization quality system.
AquaVerify
Guides and checklists for water microbiology decisions
Operational AquaVerify guides and PDF checklists for product selection, sampling, compliance, LIMS migration and partner conversations.
Direct answer
Use this collection when you need a practical next step: a guide to read, a checklist to complete and evidence to bring into a technical conversation.
- Pair each guide with its checklist when available.
- Use PDFs as preparation tools, not as validation records by themselves.
- Keep completed checklists with method, reviewer and report context.
How to use this collection
Operational AquaVerify guides and PDF checklists for product selection, sampling, compliance, LIMS migration and partner conversations.
- Choose the decision area.
- Open the guide for context.
- Download the checklist and complete it before contacting AquaVerify.
Questions this category answers
Use this collection when you need a practical next step: a guide to read, a checklist to complete and evidence to bring into a technical conversation.
- Which checklists are available?
- How should completed checklists be stored?
- Which guide helps choose an AquaVerify product?
Selected resources
Operational AquaVerify guides and PDF checklists for product selection, sampling, compliance, LIMS migration and partner conversations.
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Resource
How to choose the right AquaVerify product for microbiological water analysis
A practical guide to decide between ENUMERA, INDICA, ISO/EPA Kits, Lab Essentials and AquaVerify Cloud according to analytical objective, matrix, urgency, traceability level and operational context.
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Resource
RD 3/2023 and somatic coliphages: practical guide for water laboratories and operators
A practical resource to translate the Spanish drinking water framework and the European risk-based approach into sampling plans, somatic coliphage monitoring, treatment evidence and traceable reporting.
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Resource
ISO/IEC 17025 for water laboratories: chain of custody, CoA and digital traceability
A practical whitepaper for laboratories that need to strengthen sample control, method execution, review, reporting and customer communication without claiming automatic accreditation.
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Resource
Water Safety Plans: turning water risk into a traceable control program
A guide to structure risk-based water control from catchment to point of use, connecting hazards, control points, microbiological indicators, corrective actions and digital evidence.
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Resource
Water in food and beverage: microbiological control, batch evidence, CIP and audit readiness
A practical guide for QA/QC teams that manage ingredient water, process water, rinse/CIP water, batch release evidence and audit documentation.
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Resource
Water risk management in facilities: Legionella, terminal points and traceability
A practical guide for facilities, hotels, spas, healthcare buildings and multi-site operators that need to coordinate water risk plans, sampling, corrective actions, supplier evidence and inspections.
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Resource
ISO 19458 and microbiological water sampling: planning, collection and transport with traceability
A practical guide for laboratories, utilities, facilities, food plants, industry and agriculture teams that need to control sampling points, containers, preservation, transport, chain of custody and digital evidence.
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Resource
From Excel to LIMS: digitizing water samples, results and reports
A guide for laboratories, distributors and quality teams moving from spreadsheets and email to a traceable flow with LIMS, CoA, customer portal, inventory and operational follow-up.
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Resource
OEM and white label water testing kits: guide for distributors and partners
A commercial and technical guide to evaluate AquaVerify distribution, co-branding, white label, packaging, documentation, training, software and territorial scaling.
Downloadable checklists
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Checklist
Checklist for adding coliphages to an analytical program
Questions on monitoring objective, matrix, volume, host strain, controls, PFU results and reporting.
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Checklist
EU Directive / RD 3/2023 checklist
Preparation guide for sampling points, risk assessment, somatic coliphages, records and evidence.
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Checklist
LIMS, CoA and audit trail checklist
Evaluate whether the current workflow captures sample, method, batch, operator, review, report and customer portal.
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Checklist
Distributor and OEM checklist
Assess territory, technical support, inventory, packaging, co-branding and white label readiness.
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Checklist
Product selection checklist
Prepare a product recommendation conversation around matrix, decision type, volume and traceability.
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Checklist
RD 3/2023 somatic coliphage checklist
Organize sampling points, raw-water context, method readiness and reporting evidence.
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Checklist
ISO/IEC 17025 laboratory evidence checklist
Review chain of custody, CoA, audit trail, permissions and technical approval flow.
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Checklist
Water Safety Plan traceability checklist
Turn hazards, control points, monitoring and corrective actions into reviewable evidence.
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Checklist
Food and beverage water checklist
Connect process water, CIP, batch context, microbiology results and audit evidence.
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Checklist
Facility water risk checklist
Prepare recurring control around Legionella-oriented risk, terminal points, actions and suppliers.
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Checklist
ISO 19458 microbiological sampling checklist
Prepare sampling objectives, points, containers, preservation, transport and chain-of-custody records.
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Checklist
Excel to LIMS migration checklist
Map samples, methods, results, reviews, CoA, portal and inventory before moving to a connected workflow.
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Checklist
OEM and white label readiness checklist
Evaluate territory, packaging, documentation, training, support, software and partner launch readiness.
FAQ
Can a distributor use these guides?
Yes. They help prepare buyer, support, product and OEM conversations.