24 modules. Each implements a named obligation under the CCOA Standards of Practice, the Health Information Act or an Alberta directive — and each ends in an evidence export.
Per patient, per user, per time range — with no spreadsheet in the middle.
24 modules in seven groups, in the order a clinic needs them. Each entry links to its section below.
The substrate every other module assumes: the record is available, every action is attributed, and consent is part of the note.
Encryption, retention, the Information Manager Agreement, a live Privacy Impact Assessment and the full HIA administration programme — the artefacts a custodian has to produce.
What a practitioner may record, refer, publish or cause to occur — bounded at save time, with the evidence the CCOA expects.
Charts another clinician can read, imaging that lands on the record, health information that leaves only through a secured channel, and published copy that passes the Directive.
Fees, contracts and prepayments; policies, equipment and support staff; fitness to practice, continuing competence and concluding care — the recurring obligations of running a clinic.
An embedded assistant that drafts but never authors: off until the custodian enables it, scoped to what a human grants for one session, and recorded turn by turn in a tamper-evident ledger.
An opt-in research module for the rare clinic that conducts studies — and the rules this website itself is written under.
The substrate every other module assumes: the record is available, every action is attributed, and consent is part of the note.
A published availability objective for chart load, measured in production. When a dependency fails, the record degrades to a labelled read-only mode instead of an opaque error.
Unique accounts, custodian-configurable roles, a second factor on every new device, and an append-only audit log that records views, edits, exports, denials — and every attempt to tamper with it.
A SOAP entry cannot be finalised without signposting and consent to touch for that visit. Scoped declines, substitute decision-makers and the CCPA informed-consent version in force are part of the same record.
Encryption, retention, the Information Manager Agreement, a live Privacy Impact Assessment and the full HIA administration programme — the artefacts a custodian has to produce.
Encryption in transit and at rest with keys held separately, verified backups, a quarterly restore test on record, integrity alerts, and a disposal attestation for every medium that ever held health information.
Every chart carries a retention floor computed from SP 5.4, and deletion before the floor is blocked. The Information Manager Agreement is signed before the first record and verified against every Appendix 4 component.
The workbook renders from a live fact graph: what the platform warrants, what the clinic configured, what the custodian attested. When a fact drifts, a finding opens and the features that depend on it fail closed.
A designated HIA officer of record, public policies, tiered training, a periodic status-quo assessment, an access and correction request register with statutory deadlines, and a privacy compliance plan.
What a practitioner may record, refer, publish or cause to occur — bounded at save time, with the evidence the CCOA expects.
A configuration-driven register of every restricted activity and directive: what is authorised, what needs Registrar authorisation and evidence, what is prohibited. Charts, treatment plans and invoice lines are checked at save time.
Intake is screened against the CCOA indicator sets. Flags persist across every encounter until closed with evidence; red and orange flags block signing without a documented referral or a documented decline.
A boundary checkpoint on any sensitive-area contact, structured responses to boundary indicators, registers for dual relationships, gifts and social media, and a duty-to-report workflow to the Complaints Director.
A structured record of the harm, the conversation with the patient, the remedial care or referral, and the step taken to prevent recurrence — invokable from the chart, a critical event or a secure message.
Female genital mutilation cannot be recorded as a procedure in any clinic, under any configuration. Reasonable grounds about another regulated member open the HPA s. 127.2 report; a patient’s disclosure opens trauma-informed care instead.
Charts another clinician can read, imaging that lands on the record, health information that leaves only through a secured channel, and published copy that passes the Directive.
A practitioner-configurable exam library, reproducible findings with side tested and standard coding, validated outcome measures, ICD-10-CA diagnosis coding and a no-shorthand mode.
Every imaging requisition is attached at issuance with its metadata. Reports are filed against the requisition, unsolicited reports are triaged, and clinically significant findings queue a follow-up.
Health information leaves the chart only through a secured channel, and only once the PIA allows it. Every disclosure to a third party needs a structured authorisation and lands in the patient’s disclosure log.
Website text, social posts, brochures, recall messages and testimonials composed in the platform are checked against the Professional Communication Directive at publish time — and re-checked when the lists change.
Fees, contracts and prepayments; policies, equipment and support staff; fitness to practice, continuing competence and concluding care — the recurring obligations of running a clinic.
Dated fee schedules with legislated fees included, a provider-contract register, prepayment caps enforced, a financial-agreement composer with every mandatory clause, and an invoice engine bound to signed encounters.
Jurisdiction-aligned templates adopted per clinic, with training logs and audits, a critical event log, an equipment register with maintenance reminders, and a support-staff register that enforces the SP 4.2 blocklist.
Self- and colleague disclosure of incapacity, a cease-or-limit state that scheduling and charting honour, and a reinstatement path — with medical detail visible only to the practitioner and the disclosure roles.
A CPD log with verified attendance, a renewal-eligibility check against the Council threshold, practice-visit preparation drawing on every module’s evidence, and Committee directives tracked to deadline.
A discharge workflow that screens the reason against prohibited grounds, composes the notice with every SP 11.0 clause, sends it through the secure channel and refunds unrendered fees immediately.
An embedded assistant that drafts but never authors: off until the custodian enables it, scoped to what a human grants for one session, and recorded turn by turn in a tamper-evident ledger.
The embedded assistant is off until the custodian enables it under a current IMA and a recorded sub-processor acknowledgement. It sees no patient unless a human grants access for that session, it proposes actions it cannot execute, and every turn lands in a tamper-evident ledger.
An opt-in research module for the rare clinic that conducts studies — and the rules this website itself is written under.
An opt-in module: research proposal and ERB approval on file, the Registrar notified through the secure channel, per-patient research consent with disclosure scope, and research data segregated by role.
Every claim on this website is present tense and producible on demand. No fabricated certifications, no invented customers, no absence labels, no implementation detail — checked before every release.
85 clauses, each mapped to the module that operationalises it. Read the standard, then see what was built against it.
This index is descriptive, not legal advice. Verify the current versions of the Standards of Practice, the HIA and the CCPA document at theccoa.ca, oipc.ab.ca and ccpa-acpc.ca.