Automation for the routine. Audra for the drafting. People decide.
Every standard. Every industry. One system from first gap to certificate.
AMS implements and runs your management system, from ISO 9001 and ISO 22000 to ISO 27001, SOC 2 and 36 standards in total. It drafts the documents, captures evidence from your systems and your shop floor, and keeps everything current between audits.
What applies to you?
Describe your organization in a sentence.
An estimate from your description. A scoping call confirms scope, sites and exclusions.
Scattered records in. Audit-ready system out.
AMS reads what your organization already has, works out which clause each piece belongs to, and builds the management system around it. Hover a source to follow it through.
- Processes and SOPsWork instructions, process maps
- Cloud and IT systemsAWS, Azure, Okta, Google, M365
- Shop floor and sitesInspections, readings, photos
- People and trainingHRIS, LMS, competence records
- Suppliers and vendorsApprovals, contracts, reports
- Existing documentsManuals, policies, old audits
- Scoping
- Policy writer
- Evidence collector
- Audit assistant
- Controlled documentsPolicies, procedures, registers
- Signed evidence vaultTimestamped, mapped to clauses
- Live readiness scorePer standard, per site
- Internal audits and CAPAFindings to closure
- Certification audit packReady for your certification body
Your whole compliance program on one screen, in your team's language
Readiness per standard and per site, evidence freshness, open tasks and the next audit. Switch the language below to see the same dashboard the way a plant manager in Monterrey, Lyon or Riyadh would.
Compliance overview
Readiness by standard
Evidence collected per week
Sites
- Plant 1, Dallas92%
- Plant 2, Houston81%
- Warehouse, Austin76%
Coming up
- Internal audit, clause 8
- Management review
- Document reviews due (3)
Agent activity
- Filed evacuation drill photos, Plant 24 min ago
- Drafted the aspects and impacts register for review22 min ago
- Reminded 3 supplier owners about overdue evaluations1 h ago
- Flagged a thermometer calibration expiring in 14 days3 h ago
Works in the languages your sites speak
Every user picks their own interface language. Policies, procedures, audit reports and corrective action requests can be produced in each site's language, while the audit trail stays the same underneath. Right-to-left scripts are fully supported.
Languages with a dark outline are live in the dashboard above. Select one to try it.
See AMS at work
Real screens from a food manufacturer running ISO 9001, ISO 14001, ISO 45001 and ISO 22000 across three sites. Pick a screen.
Readiness by standard and site
| Plant 1 Dallas | Plant 2 Houston | Warehouse Austin | |
|---|---|---|---|
| ISO 9001 | 96% | 88% | 90% |
| ISO 14001 | 84% | 71% | 80% |
| ISO 45001 | 82% | 68% | 79% |
| ISO 22000 | 93% | 89% | n/a |
Today's briefing
- 1 blocker: ISO 45001 8.2 at Plant 2. The last evacuation drill was 104 days ago.
- 2 warnings: waste manifest for September missing; thermometer TH-07 calibration expires in 14 days.
- Done overnight: 38 system checks passed, 6 photos filed from the field app, 3 supplier owners reminded.
- Next: schedule the Plant 2 drill with M. Ortiz before the stage 2 audit.
Next actions
- MORun evacuation drill, Plant 2ISO 45001 8.2 · ISO 14001 8.2Due in 5 days
- SKApprove aspects and impacts register v2ISO 14001 6.1.2Drafted by Audra
- JLCalibrate TH-07 cold room thermometerISO 22000 8.7 · ISO 9001 7.1.5Due in 14 days
- PRClose NC-04: supplier evaluation overdueISO 9001 8.4Evidence attached
Plant 2 is at 71% for ISO 14001. Four things stand between you and stage 2:
- 6.1.2 Aspects and impacts: register drafted from your 2025 environmental report, waiting for approval by S. Kim.
- 9.1.1 Monitoring: September waste manifest not received. I emailed the contractor on Monday.
- 8.2 Emergency preparedness: no spill drill on record in the last 12 months.
- 9.2 Internal audit: clause 8 not yet audited this cycle. Suggested auditor: R. Diaz (trained, independent of Plant 2).
Closing all four takes readiness to about 92%. The drill also covers ISO 45001 8.2.
All measuring equipment used for product conformity is listed in the equipment register with a unique ID. ISO 9001 7.1.5
All measuring equipment is calibrated every six months against traceable standards. ISO 9001 7.1.5.2
Cold room thermometers are verified daily at the start of each shift. ISO 22000 8.7
Equipment found out of tolerance is quarantined, and products measured since the last good check are assessed.
Audra flagged a claim
Calibration certificates exist for 41 of 48 gauges. Seven are overdue, so "every six months" can't be proven at audit.
Approval: Quality Manager · then published to all sites in English, Spanish and Arabic
1System checks
Monday 06:00 · 38 of 39 passed
- MFA enforced for admins M365
- Daily backup completed Veeam
- Training overdue: 0 people LMS
- Supplier ratings current ERP
- Leaver account still active Entra ID
2Screen capture
ERP user roles page · no API
- Capture1440×900, timestamped
- Redact2 personal fields masked
- Quality checkreadable, correct page
- SignSHA-256 + trusted timestamp
- FileISO 27001 A.5.18
3Guided procedure
Quarterly backup restore test · run 4
- DTRestore last backup to test server
- AutoCompare record counts: 2,418,902 match
- CFIT Manager signs off
- AutoFile signed record to A.8.13
Plus email and Teams/Slack/WhatsApp: forward a file and AMS files it against the right requirement. Freshness is checked daily: fresh, due at 90 days, expired at 120.
Monthly fire extinguisher check
- FE-01 Loading bay photo
- FE-02 Packing line 3 photo
- FE-03 Cold store: pressure low photo + note
- FE-04 Boiler room
Built for shop floors, labs and sites
- Checklists, photos, readings and signatures from a phone or tablet
- Works offline and syncs when back in range
- Every photo stamped with time, user and location
- Failed items open a corrective action automatically
- In each worker's own language
FE-03 created CA-118, assigned to Maintenance, due in 7 days. Counts toward ISO 45001 8.2 and ISO 22000 8.4.
The same evidence also satisfies
- ISO 9001 8.5.1 Control of production
- FSSC 22000 2.5.1 Food safety requirements
- BRCGS 4.6 Equipment monitoring
Risk and opportunity register
| ID | Risk | Standard | Inherent | Residual | Owner |
|---|---|---|---|---|---|
| R-014 | Allergen cross-contact on shared line 3 | ISO 22000 | 20 | 6 | Quality |
| R-009 | Ammonia leak in refrigeration plant | ISO 45001 · 14001 | 20 | 10 | Maintenance |
| R-021 | Single supplier for packaging film | ISO 9001 | 15 | 9 | Purchasing |
| R-027 | Ransomware on production scheduling | ISO 27001 | 16 | 6 | IT |
Internal audit programme 2026
- Clause 4 to 7, all sites
- Clause 8, Plant 1
- Clause 8, Plant 2
- Clause 9 to 10 + management review
Findings
- NC-04 Supplier evaluation overdueISO 9001 8.4Closed
- NC-06 Drill not performed, Plant 2ISO 45001 8.2Open
- OFI-03 Legal register review datesISO 14001 9.1.2Noted
Stage 2 audit pack
Documents, evidence manifest, internal audit reports, management review minutes and NC responses, signed and indexed.
A week of compliance, mostly on autopilot
Scheduled automation does the checking, chasing and filing. Audra prepares drafts where they help, and your team approves.
- Monday · 06:00System checks
Identity, backups, training, ERP and lab systems checked against their requirements.
38 of 39 passed - Every day · 06:00Freshness check
Every record checked against its window: fresh, due at 90 days, expired at 120.
3 records due soon - Every day · 06:30Briefing
Readiness, blockers and the one next step, posted to email, Teams, Slack or WhatsApp.
86% · 1 blocker - Every dayFollow-ups
Owners reminded before work is due and escalated when it's late, in their language.
4 reminders sent - When something failsFix suggested
Each failed check or field item comes with the fix and opens a corrective action.
CA-118 opened - Before the auditAudit pack
Signed, indexed pack exported for the certification body you choose, or shared through a read-only auditor portal.
Ready for stage 2
Why teams move to AMS
Most compliance software tracks the work and hands it back to you. AMS does the work, across every standard you run, with people behind it.
| Topic | Spreadsheets and typical compliance tools | AMS |
|---|---|---|
| Standards | One tool per area, often only security frameworks | ✓ 36 standards on one system: quality, environment, safety, food, medical, security, AI |
| Who does the work | A dashboard of tasks assigned to you | ✓ Automation checks, chases and files; Audra prepares drafts; you approve |
| Evidence | API checks, then manual screenshots and uploads | ✓ System checks, screen capture, guided procedures, email and chat, offline field capture |
| Shop floor, wards, labs | Paper checklists typed in later | ✓ Phone checklists with photos, offline, in each worker's language |
| Policies | Templates that promise more than you do | ✓ Written from your real records; unproven claims flagged before the auditor sees them |
| Change and document control | Email approvals, old versions still in use | ✓ Impact checked, approvals routed, staff retrained, old versions withdrawn |
| Same record, many standards | The same evidence collected again per standard | ✓ One record counts toward every clause it meets |
| Proof | A folder of files | ✓ Signed, timestamped evidence traced from policy sentence to proof |
| Certification audit | Files emailed to the auditor in pieces | ✓ A signed, indexed audit pack and a read-only auditor portal, for any certification body |
| Implementation | Software only, or a separate consultant | ✓ Our consultants configure, train and stay |
| Languages and hosting | Usually English, cloud only | ✓ 12+ languages including right-to-left; cloud, private cloud or your own servers |
Assistant Built into AMS, used where it helps
Meet Audra. It prepares the drafts. Your team decides.
Most of AMS is plain automation and rules: schedules, reminders, checks and workflows. Audra steps in only where drafting helps, preparing documents, summaries and answers for a person to review. Nothing is published or closed without approval.
- Drafts only. Nothing is published, closed or sent without a named person's approval.
- Shows its sources. Every answer and draft links to the records it used.
- Leaves a trail. Every action is logged, so auditors can see what Audra drafted and who approved it.
- No client data to outside AI. Your records and client information never go to any external AI service, and are never used to train AI models.
- ✎Drafts documents
Policies, procedures and registers from your records, for your review
Audra prepares - ↻Suggests updates
Lists what a change affects and drafts the revisions
Audra prepares - ?Answers questions
"What's missing for stage 2?" in plain words, with sources
Audra prepares - ◎Checks evidence
System checks and freshness checks on a schedule
Automation - ➤Sends reminders
Owners reminded before work is due, escalated when late
Automation - ✔Approves
Every draft, closure and publication
Your team decides
Your data is protected by design
AMS is built and run under our own ISO/IEC 27001, ISO/IEC 42001 and ISO 9001 certified management systems.
- ✦No client data to outside AI
Audra never sends your records or client information to any external AI service. It runs privately inside your own environment, personal data is masked first, and nothing is ever used to train AI models.
- 🔒Encrypted everywhere
Encrypted in transit and at rest, including backups. Encryption keys are managed separately from the data.
- 🌍Stored where your law requires
Choose the hosting region, or run it on your own servers, so you can meet local data protection laws such as GDPR, India's DPDP Act and Gulf PDPL rules.
- ◐Masked by default
Names, contact details and other personal data are masked for every role that doesn't need them, on screen and in exports.
- ≡Fully audited
Every view, change, export and approval is logged with who, what and when, and can be reviewed by your auditors.
- ⚿Your data stays yours
You own your data. Export it any time, and it is deleted on exit, with written confirmation.
- ⊟Separate by design
Each customer's data is isolated. Derasar Designs staff can't open it without your written, time-limited permission.
Fixes the everyday work, not just the audit
The same headaches show up in every management system, in every industry. Here is how AMS handles each one, with Audra preparing drafts where it helps.
Policy and document updates
Old versions on shared drives. Nobody knows which one is current.
One controlled library. Review dates tracked, staff acknowledge each new version, old versions withdrawn automatically.
Audra drafts the revision and lists who must re-read it.
Change management
A new machine, supplier or recipe goes in, and the paperwork catches up months later.
Every change gets an impact check across documents, risks, training, suppliers and validation before approval.
Audra finds the 9 documents and 2 risk entries a change affects.
Training and competence
Spreadsheets of who was trained on what, out of date by the next audit.
Training matrix by role, linked to document versions. Retraining assigned the moment a procedure changes.
AMS reminds people in their own language and records completion automatically.
Deviations and nonconformances
Problems fixed on the floor and never recorded, so they come back.
Log in seconds from a phone, with photos. Severity rules decide the route: correction, investigation or CAPA.
AMS flags repeats across sites; Audra can draft a root-cause summary.
Corrective actions (CAPA)
Actions closed on paper with no proof they worked.
Root cause, actions, owners, due dates and an effectiveness check before closure.
AMS schedules the effectiveness check and asks the owner for proof.
Customer complaints
Complaints sit in email inboxes; trends are invisible.
Complaints logged from email or portal, classified, investigated and answered on time, with trends by product and site.
Audra drafts the customer reply and links the complaint to batch and supplier.
Supplier quality
Approved supplier lists with expired certificates nobody noticed.
Approval, scorecards, certificate expiry and supplier audits in one record per supplier.
AMS requests renewed certificates automatically, 60 days before expiry.
Equipment, calibration and maintenance
Overdue calibration found by the auditor, not by you.
Equipment register with calibration and maintenance schedules, certificates and out-of-tolerance handling.
AMS flags results measured with an overdue gauge and opens a review for QA.
Internal audits
Audit programme in a spreadsheet; findings chased by email.
Risk-based programme, checklists per clause with evidence pre-linked, findings tracked to closure.
Audra drafts the checklist; AMS suggests auditors who are independent of the area.
Management review
Two weeks of copying numbers into slides.
Every required input collected live: audits, KPIs, complaints, risks, supplier performance.
Audra prepares the pack and records decisions as actions.
New laws and standard revisions
A standard changes and nobody notices until the transition deadline.
Legal register and standard revisions tracked, with gap lists and transition plans.
Audra lists exactly which clauses and documents a revision affects.
Risk and opportunities
A risk register filled in once for the auditor.
Risks linked to processes, incidents and changes, re-scored when something happens.
AMS opens a risk review after an incident or a failed check.
Built in depth for your industry
AMS arrives with the records, workflows and checklists your sector already uses, so you start from how your industry works, not from a blank system.
What hurts today
- Temperature and CCP logs on paper, filled in at the end of the shift
- Allergen changeovers and cleaning not verified
- Mock recalls take days because lot data sits in three systems
What AMS captures
- CCP monitoring, from loggers or a phone, with alerts outside limits
- Sanitation, allergen changeover and pre-operational checks
- Environmental monitoring swabs and pest control visits
- Glass and brittle plastics, foreign body and metal detector checks
- Lot traceability one step up and one step down
Ready-made workflows
- HACCP plan and hazard analysis
- Mock recall in minutes, with a timed report
- Supplier approval with certificate expiry tracking
- Customer complaint to batch investigation
Audra: "Cold room 2 read 7.4 °C at 02:00. QA notified to hold the product; deviation DV-212 drafted."
What hurts today
- Accreditation preparation becomes a last-minute scramble
- Incidents and near misses go unreported or unanalysed
- Equipment maintenance and staff credentials expire quietly
What AMS captures
- Incident and near-miss reports, including medication errors
- Infection control and hand hygiene audits on a tablet
- Biomedical equipment maintenance and calibration
- Staff credentials, licences and mandatory training
- Patient feedback and complaints, fire and code drills
Ready-made workflows
- Accreditation standards mapped to evidence, ward by ward
- Root cause analysis for serious incidents
- Policy acknowledgement by department and role
- Patient data protection checks
Audra: "Ward 3 hand hygiene compliance fell to 78%. Re-audit proposed for Thursday; ward lead notified."
What hurts today
- Customer complaints answered late; 8D reports written from scratch
- Control plans and PFMEAs out of step with the line
- Safety inspections and energy data kept outside the system
What AMS captures
- Nonconforming product, scrap and rework with photos
- Gauge calibration and measurement system analysis
- Preventive maintenance and breakdowns
- Safety walks, lockout checks and near misses
- Energy meter readings and environmental aspects
Ready-made workflows
- 8D for customer complaints, with containment in 24 hours
- PFMEA and control plan linked to changes
- PPAP and first article records
- Supplier PPM scorecards and audits
Audra: "Third torque complaint from the same line in 30 days. 8D drafted and linked to change CR-044."
What hurts today
- Deviations and CAPA slow batch release
- Change control spread across email and paper forms
- Training records don't match the current SOP versions
What AMS captures
- Deviations with impact assessment on batches
- Change control with risk assessment and approvals
- SOP versions linked to role-based training
- Design history and risk management files
- Complaints and post-market feedback
Ready-made workflows
- Deviation to CAPA to effectiveness check
- Change control with documents and retraining
- Supplier qualification and quality agreements
- Risk management per ISO 14971
Audra: "Change CC-031 affects 4 SOPs and 26 operators. Drafts and retraining are ready for QA approval."
Validation support for regulated GxP use (such as 21 CFR Part 11 and EU Annex 11) is discussed per project.
What hurts today
- Method validation and uncertainty spread across workbooks
- Proficiency testing results not followed up
- Reagent lots and equipment status hard to prove
What AMS captures
- Method validation and verification records
- Measurement uncertainty budgets
- Proficiency testing results and follow-up
- Equipment calibration, reagent and reference material lots
- Analyst competence and witnessing
Ready-made workflows
- Nonconforming work and report recalls
- Impartiality and confidentiality reviews
- Complaint handling for test results
- Internal audit by technical area
Audra: "PT round 2026-3 failed for lead in water. Results since June under review; analyst retraining assigned."
What hurts today
- Security questionnaires slow down every sale
- Access reviews and offboarding missed
- AI systems in use with no inventory or risk assessment
What AMS captures
- Identity, cloud, code and backup checks on a schedule
- Access reviews and joiner, mover, leaver records
- Vendor risk and data processing agreements
- AI system inventory and impact assessments
- Incidents and continuity tests
Ready-made workflows
- Security questionnaires answered from your controls
- Quarterly access reviews with sign-off
- Change management linked to code and tickets
- Trust page built from live evidence
Audra: "Leaver account still active in Entra ID. Ticket drafted for IT; the check re-runs tonight."
Collect evidence once. Satisfy every standard it touches.
ISO management standards share the same backbone. AMS maps each record to every clause it meets, so a single drill report or training log counts across your whole system.
From first conversation to certificate
Eight stages, grouped into four phases. Scroll through to see what AMS does in each one.
-
1 Phase 1 of 4
Discover
We learn your industry, sites and processes, decide which standards apply, then score every clause for readiness using interviews, your documents and read-only system scans.
Stages: scope, gap assessment
-
2 Phase 2 of 4
Build
AMS drafts policies, procedures and registers from what it actually found, flags any commitment you can't yet prove, and turns every requirement into an owned task.
Stages: document build, implement
-
3 Phase 3 of 4
Prove
Evidence arrives on schedule from systems, screens, guided procedures and the shop floor. Internal audits run inside the platform with findings tracked to closure.
Stages: evidence capture, internal audit
-
4 Phase 4 of 4
Certify and maintain
Your certification body receives a structured audit pack. After certification, reviews, standard revisions and surveillance prep keep running in the background.
Stages: certification audit, maintain
- 4 Context82%
- 5 Leadership64%
- 6 Planning38%
- 7 Support55%
- 8 Operation47%
- 9 Evaluation21%
- 10 Improvement30%
- Quality policyApproved
- Aspects and impacts registerApproved
- Emergency preparedness planDrafting
- Calibration procedure1 claim unproven
- Legal and compliance registerOwner review
- Evacuation drill, Plant 2Field app, 6 photos45001 8.2
- MFA enforced on adminsOkta check27001 A.5.17
- Torque wrench calibrationCertificate upload9001 7.1.5
- Waste manifest, SeptemberEmail to vault14001 9.1
- Surveillance auditin 11 months
- Document reviews due3 this quarter
- Standard revisions tracked2 upcoming
What changes when AMS runs your compliance
- Spreadsheets and shared drivesOne controlled system
- Evidence chased the week before an auditEvidence captured as the work happens
- A separate consultant for each standardOne system for all of them
- Audit files emailed in piecesA structured pack sent to your certification body
Evidence that stays current on its own
Integrations only reach part of a management system. The rest lives on factory floors, in labs and in admin consoles, so AMS captures it four ways.
- System checks
- Cloud, identity, HR, ERP and lab systems checked on a schedule.
- Screen capture
- Settings pages with no API, captured, redacted and re-captured before they go stale.
- Guided procedures
- Backup restores, emergency drills and calibration checks recorded step by step.
- Field capture
- Photos, readings and checklists from the shop floor on a phone, even offline.
Quarterly evacuation drill
Integrity hash 7f3a 91c2 e04b 5d18
Works with any certification body
AMS gets you ready for certification. The certification itself stays with an independent, accredited certification body of your choice.
What you get
- A signed, indexed audit pack in standard formats (PDF, spreadsheet and a verification manifest)
- A read-only auditor portal you can open to any auditor, for a set period
- Responses to nonconformities with evidence attached
- The same pack whichever certification body you choose
How we keep it independent
- Derasar Designs does not certify anyone, and is not a certification body
- We never recommend or steer you to a particular certification body
- Your data is yours: no certification body sees it unless you share it
- Consulting and certification stay separate, as ISO/IEC 17021-1 requires of certification bodies
36 standards and frameworks, one system
Start with one. Add the next without rebuilding what you already have.
Quality and operations
Environment and energy
Health, safety and resilience
Information security, privacy and AI
- ISO/IEC 20000-1IT service management
- ISO/IEC 27001Information security
- ISO/IEC 27701Privacy information management
- ISO/IEC 42001AI management
- SOC 2Trust services criteria
- SOC 1Controls over financial reporting
- PCI DSSPayment card security
- HIPAAHealth information protection
- GDPREU data protection
- NIST CSFCybersecurity framework
- HITRUSTHealthcare security assurance
- DORAEU digital operational resilience
- NIS 2EU network and information security
Food safety
Medical devices and laboratories
Built around how your industry actually works
The evidence a bakery needs looks nothing like what a SaaS company needs. AMS knows the difference.
Food and beverage
HACCP plans, CCP monitoring, traceability and recall drills.
ISO 22000, FSSC 22000, BRCGSMedical devices
Risk files, design history, supplier controls and CAPA.
ISO 13485, risk managementManufacturing
Calibration, maintenance, hazard assessments and energy metering.
ISO 9001, 14001, 45001, 50001Software and AI
Access reviews, change management, model inventories and vendor risk.
ISO 27001, SOC 2, ISO 42001Healthcare
Patient data safeguards, incident logs and continuity plans.
HIPAA, HITRUST, ISO 22301Laboratories
Method validation, uncertainty, proficiency testing and equipment records.
ISO/IEC 17025, ISO 15189Automotive and aerospace
Core tools, control plans, first article inspection and TISAX.
IATF 16949, AS9100, TISAXEducation
Learner requirements, curriculum controls and feedback loops.
ISO 21001, ISO 9001
Software, with people behind it
Use AMS on your own, or have our implementation team run the program with you.
Platform
AMS for your internal team: documents, evidence, audits and dashboards across every standard you run.
Implementation
Our consultants scope, build and run the program to certification, with AMS doing the repetitive work.
Managed compliance
After certification, we keep it running: reviews, internal audits, surveillance prep and standard transitions.
Two ways to run it
Start on a subscription and move to your own installation whenever you need to.
Cloud subscription
Monthly or annual, priced by users and by what you run: standards in AMS, offices, schemes or auditors in CABAMS. Hosted in the region your data law requires.
- Start with what you need, add users or standards any time
- Updates, backups and support included
- Encrypted, masked and fully audited
Dedicated to your organization
Your own installation, hosted for your organization only: in a private cloud in your chosen region, or on your own servers.
- Single-tenant: no data shared with any other customer
- Your security rules, single sign-on and integrations
- A named success manager and agreed service levels
AMS questions
Something else on your mind? Ask us directly
What is AMS?
AMS (Audit Management System) helps an organization build, run and maintain its management systems: documents, risks, training, evidence, internal audits, corrective actions and management review, through to the certification audit and every year after.
Which standards does AMS cover?
36 standards and frameworks on one system, including ISO 9001, ISO 14001, ISO 45001, ISO 22000, ISO 13485, ISO/IEC 27001, ISO/IEC 42001, SOC 2, HIPAA, GDPR and sector schemes such as IATF 16949 and BRCGS.
Does AMS use AI?
Only where it helps. Most of AMS is automation and rules: schedules, reminders, checks and workflows. The assistant, Audra, prepares drafts such as documents, update lists and answers, and a named person approves everything before it is published, closed or sent. You can switch Audra off.
Is our data sent to AI or anyone outside?
No client data goes to any outside AI service, and nothing is used to train AI models. Data is encrypted in transit and at rest, masked for roles that don't need it, and hosted in the region your data protection law requires, or on your own servers.
Does AMS or Derasar Designs certify us?
No. Derasar Designs is not a certification body. AMS gets you ready and prepares a signed audit pack and a read-only auditor portal for the independent, accredited certification body you choose.
Can we run several standards and sites together?
Yes. Standards share one integrated system, so one record counts toward every requirement it meets, with readiness tracked per standard and per site.
Does it work on the shop floor without internet?
Yes. The field app records checklists, photos, readings and signatures offline and syncs when back in range, in each worker's own language.
How is AMS priced?
As a subscription, monthly or annual, priced by the number of users and the standards you run. Organizations that need their own environment can choose Enterprise: a dedicated installation hosted for them only, in their region or on their own servers.
Can consultants use AMS for several clients?
Yes. Consultants can manage separate client workspaces from one login, with each client's data kept apart.
Which languages are supported?
More than 12 interface languages, including right-to-left scripts such as Arabic. Documents can be produced in each site's language.