{"id":58454,"date":"2026-11-01T11:15:47","date_gmt":"2026-11-01T11:15:47","guid":{"rendered":"https:\/\/www.bridge-global.com\/blog\/?p=58454"},"modified":"2026-11-05T04:04:40","modified_gmt":"2026-11-05T04:04:40","slug":"ai-clinical-documentation-right-tool","status":"publish","type":"post","link":"https:\/\/www.bridge-global.com\/blog\/ai-clinical-documentation-right-tool\/","title":{"rendered":"AI Clinical Documentation: How to Choose the Right Tool"},"content":{"rendered":"<p>AI clinical documentation turns encounter information into draft clinical content, and healthtech product teams should evaluate its accuracy, review burden, and fit with the EHR workflow. AI clinical documentation turns encounter information into draft notes, code suggestions, or summaries for clinician review, but the buying decision is whether supervising those drafts is safer and lighter than writing the documentation yourself. Choose the tool against a named clinical workflow, its correction burden, and its route into the EHR.<\/p>\n<h2>What AI Clinical Documentation Actually Covers<\/h2>\n<p><strong>Four documentation jobs and what to verify first<\/strong><\/p>\n\n\n<figure class=\"wp-block-table\"><table><tr>\n<th>Job<\/th>\n<th>What it produces<\/th>\n<th>What to check first<\/th>\n<\/tr>\n<tr>\n<td>Ambient scribing<\/td>\n<td>Draft note built from the recorded visit<\/td>\n<td>Omissions, invented findings and the consent workflow<\/td>\n<\/tr>\n<tr>\n<td>Structured note drafting<\/td>\n<td>SOAP or specialty-template draft<\/td>\n<td>Template fit, medication and allergy accuracy<\/td>\n<\/tr>\n<tr>\n<td>Coding suggestions<\/td>\n<td>Diagnosis and procedure code candidates<\/td>\n<td>Documentation support for each suggested code and clinician sign-off<\/td>\n<\/tr>\n<tr>\n<td>Summaries<\/td>\n<td>After-visit instructions, referral or handoff text<\/td>\n<td>Clinical accuracy of follow-up actions and patient-facing wording<\/td>\n<\/tr>\n<\/table><\/figure>\n\n\n<p>Name the job before evaluating the product. A conversation transcript, a specialty note, and patient-facing discharge instructions need different acceptance tests. A coding suggestion also needs evidence in the documentation, not merely a plausible match to something mentioned during the visit.<\/p>\n<p><figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.bridge-global.com\/blog\/wp-content\/uploads\/2026\/11\/ai-clinical-documentation-infographic.jpg\" alt=\"A diagram explaining that AI clinical documentation software creates draft notes, billing codes, and patient encounter summaries.\" \/><\/figure>\n<\/p>\n<p>For capture mechanics, our guides to ambient AI for healthcare, ambient clinical workflows, and ambient clinical intelligence provide adjacent context. The AI-powered clinical documentation guide covers the broader category; the engineering decision here is choosing, integrating, and validating a specific tool.<\/p>\n<p>A <a href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC12513689\/\" target=\"_blank\" rel=\"noopener\">2025 synthesis of digital-scribe studies<\/a> reported that clinicians using one system for more than 60% of visits reduced documentation time per encounter by 28.8%, approximately 1.8 minutes. That&#039;s an implementation result, not a procurement guarantee.<\/p>\n<p>Don&#039;t blend specialties or adoption levels into one return-on-investment assumption. Establish whether the candidate can safely perform the documentation job inside your actual EHR workflow, then measure the benefit.<\/p>\n<h2>Build, Buy or Embed the Documentation Layer<\/h2>\n<p>Start with who owns clinical risk, not which model generates the nicest SOAP note. The sourcing path changes engineering responsibilities, but it doesn&#039;t remove the need for a clinical owner.<\/p>\n<p><strong>Build, buy or embed<\/strong><\/p>\n\n\n<figure class=\"wp-block-table\"><table><tr>\n<th>Path<\/th>\n<th>Fits when<\/th>\n<th>Risk that stays with you<\/th>\n<\/tr>\n<tr>\n<td>Build<\/td>\n<td>Note quality is the product and the team can run clinical safety, NLP and EHR write-back<\/td>\n<td>Long validation and continuous model monitoring<\/td>\n<\/tr>\n<tr>\n<td>Buy a scribe<\/td>\n<td>A provider wants less after-hours documentation inside an existing EHR<\/td>\n<td>Lock-in, weak specialty fit and unclear use of audio for training<\/td>\n<\/tr>\n<tr>\n<td>Embed a model or API<\/td>\n<td>A healthtech product already owns the clinical workflow<\/td>\n<td>Prompts, context, audit trail and any device or AI Act positioning<\/td>\n<\/tr>\n<\/table><\/figure>\n\n\n<p>Build when the differentiation depends on context assembly, specialty schemas, and documentation behavior. Budget for the speech pipeline, clinical evaluation sets, monitoring and operational support, not just inference.<\/p>\n<p>Buying makes sense when a provider wants workflow relief without becoming a documentation-platform operator. Test the vendor&#039;s specialty boundaries and contractual data terms before accepting the convenience of a packaged application.<\/p>\n<blockquote>\n<p>Buy the replaceable capability. Own the controls that determine whether your clinicians can trust and sign its output.<\/p>\n<\/blockquote>\n<p>For a virtual-care or specialty SaaS company, embedding can keep drafting inside the existing product. Your team still chooses what context leaves the platform, how corrections persist, and what users are told the feature does.<\/p>\n<p>A practical split is to procure transcription and drafting while implementing consent, review, audit, and write-back controls yourself. Scope <a href=\"https:\/\/www.bridge-global.com\/services\/custom-software-development\">custom software development<\/a> separately from <a href=\"https:\/\/www.bridge-global.com\/services\/artificial-intelligence-development\">AI development services<\/a>, and make the <a href=\"https:\/\/www.bridge-global.com\/service-models\/ai-transformation-framework\">AI implementation roadmap<\/a> start with workflow discovery. Compare <a href=\"https:\/\/www.bridge-global.com\/service-models\">software development service models<\/a> against who will maintain those controls after launch.<\/p>\n<p>No sourcing decision is complete until the signed note has a named destination in the EHR.<\/p>\n<h2>A Scorecard for AI Clinical Documentation Tools<\/h2>\n\n\n<figure class=\"wp-block-table\"><table><tr>\n<th>Criterion<\/th>\n<th>What to verify<\/th>\n<th>Red flag<\/th>\n<\/tr>\n<tr>\n<td>Accuracy and hallucination checks<\/td>\n<td>Specialty-labelled set tracking omissions, invented findings, medications, allergies and unsupported diagnoses by severity<\/td>\n<td>A single demo accuracy percentage with no error taxonomy<\/td>\n<\/tr>\n<tr>\n<td>Specialty coverage<\/td>\n<td>Results on your visit types, languages and acuity mix<\/td>\n<td>A primary-care score applied unchanged to ED, psychiatry or procedures<\/td>\n<\/tr>\n<tr>\n<td>EHR write-back<\/td>\n<td>Draft opens in the note the clinician already signs, with edit and version history<\/td>\n<td>Copy-paste into free text or a parallel note store<\/td>\n<\/tr>\n<tr>\n<td>Latency<\/td>\n<td>Draft usable during the visit or before the next patient<\/td>\n<td>Batch notes that arrive after the clinician has left<\/td>\n<\/tr>\n<tr>\n<td>Privacy and data residency<\/td>\n<td>Named subprocessors, processing region, audio retention and a no-training default<\/td>\n<td>Unclear whether audio or PHI trains a shared model<\/td>\n<\/tr>\n<tr>\n<td>Patient consent<\/td>\n<td>Visible recording state, a refusal path that doesn&#039;t worsen care, and a logged decision<\/td>\n<td>A verbal yes in the hallway treated as sufficient<\/td>\n<\/tr>\n<tr>\n<td>Pricing model<\/td>\n<td>A forecastable unit such as clinician or encounter, with review effort stated as an assumption<\/td>\n<td>Per-note fees that ignore correction time<\/td>\n<\/tr>\n<\/table><\/figure>\n\n\n<p>Use this as a pass-fail scorecard, not a weighted demo contest. A candidate that fails safety or write-back shouldn&#8217;t recover through attractive pricing or an impressive interface.<\/p>\n<h3>Ask for evidence you can reproduce<\/h3>\n<p>Provide representative encounters with clinician-approved reference notes. Require vendors to show both acceptable output and failure cases, including negation, speaker attribution, medication changes, and ambiguous follow-up instructions.<\/p>\n<p>For latency, measure from the end of usable capture to an editable draft in the clinician&#8217;s workflow. A fast generation endpoint doesn&#8217;t compensate for slow context retrieval, failed mapping, or an additional application login.<\/p>\n<p>Request a quote that separates licensing, integration, support, storage, and usage allowances. Treat reviewer time as an explicit operating-cost assumption rather than counting every generated note as saved work.<\/p>\n<h3>Consent is a product test<\/h3>\n<p>In a <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/40694347\/?fc=20250608055056&amp;ff=20250723105846&amp;v=2.18.0.post9+e462414\" target=\"_blank\" rel=\"noopener\">2025 ambulatory-care study<\/a>, consent was 81.6% after basic information, but 55.3% when disclosures included AI capabilities, data storage and corporate involvement. Patients also distinguished responsibility for medical errors from responsibility for security breaches.<\/p>\n<p>That makes a consent checkbox insufficient. Test whether patients can explain what&#8217;s recorded, who accesses it, and what happens when they refuse. Include interpreters, carers and shared encounters in the workflow design.<\/p>\n<p>Keep the explanation clear and complete even if the opt-in rate falls.<\/p>\n<p>Shortlist candidates that can demonstrate these behaviors in your environment, not merely promise them in a roadmap.<\/p>\n<h2>EHR Write-Back Patterns for Clinical Notes<\/h2>\n<p>Treat integration as a controlled transition from provisional draft to signed clinical content. Sending text into an EHR isn&#8217;t the same as placing it in the correct encounter, with the correct status and accountable signer.<\/p>\n<h3>Choose the route into the chart<\/h3>\n<p><strong>EHR vendor API or app marketplace:<\/strong> Prefer a supported native-note route when available. Verify the actual operations exposed: creating a draft, updating it, preserving edits, and handing it to the clinician for signature. Plan for vendor-specific objects, permissions, and release changes.<\/p>\n<p><strong>FHIR document exchange:<\/strong> Evaluate <code>DocumentReference<\/code> for document indexing and references, or <code>Composition<\/code> where structured document assembly fits the receiving system. Don&#8217;t assume either resource automatically becomes an editable native note; test the EHR&#8217;s supported profile and rendering behavior.<\/p>\n<p><strong>Hybrid integration:<\/strong> A capture service can hold encounter material while middleware maps the draft and the EHR API performs the final write. This separates capture from record management, but requires explicit reconciliation across systems.<\/p>\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.bridge-global.com\/blog\/wp-content\/uploads\/2026\/11\/ai-clinical-documentation-ehr-patterns.jpg\" alt=\"A diagram illustrating three EHR write-back patterns for clinical notes, highlighting API usage, embedded workflows, and review pathways.\" \/><\/figure>\n<h3>Test failures before the happy path<\/h3>\n<ul>\n<li>\n<p><strong>Authorship:<\/strong> Distinguish the drafting service from the clinician responsible for the signed note.<\/p>\n<\/li>\n<li>\n<p><strong>Retries:<\/strong> Use stable encounter and document identifiers so retries don&#8217;t create duplicate notes.<\/p>\n<\/li>\n<li>\n<p><strong>Partial failure:<\/strong> Queue and reconcile cases where capture succeeds but write-back fails.<\/p>\n<\/li>\n<li>\n<p><strong>External copies:<\/strong> Inventory audio, transcripts, drafts, and logs that remain outside the EHR.<\/p>\n<\/li>\n<\/ul>\n<p>Use SMART on FHIR when the application needs an in-chart launch and authorized context. Add DICOM-related work when documentation must reference imaging objects; leave it out of the default scribe scope.<\/p>\n<p>Our FHIR integration services guide, <a href=\"https:\/\/www.bridge-global.com\/blog\/electronic-health-records-integration\/\">electronic health records integration guide,<\/a> and <a href=\"https:\/\/www.bridge-global.com\/healthcare\/tools-and-integrations\">healthcare integrations<\/a> provide integration context. The acceptance test remains concrete: the clinician can correct a sentence and sign without leaving the EHR.<\/p>\n<h2>Safety Gates Before a Clinician Signs<\/h2>\n<p>A <a href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC12973079\/\" target=\"_blank\" rel=\"noopener\">review of ambient-scribe evaluations<\/a> describes a pilot involving 31 physicians and 7,545 clinic notes, in which 5.3% of evaluated AI-generated notes contained an error judged capable of serious harm if left uncorrected, while 94.7% were free from significant errors. Those findings support treating every generated note as provisional, not automatically finalized clinical content.<\/p>\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.bridge-global.com\/blog\/wp-content\/uploads\/2026\/11\/ai-clinical-documentation-medical-ai.jpg\" alt=\"A clinician reviewing an AI-generated draft medical note on a laptop screen in a clinical office setting.\" \/><\/figure>\n<p>The clinician should see the draft alongside relevant encounter context, correct or reject it, and deliberately approve the final text. Preserve model and template versions, the generated draft, subsequent edits, and the signer&#8217;s identity without retaining source material beyond the approved retention policy.<\/p>\n<h3>Pre-signature safety checklist<\/h3>\n<ul>\n<li>\n<p><strong>Completeness:<\/strong> Check missing symptoms, relevant negatives, and follow-up actions.<\/p>\n<\/li>\n<li>\n<p><strong>Unsupported content:<\/strong> Flag invented findings and diagnoses the encounter doesn&#8217;t support.<\/p>\n<\/li>\n<li>\n<p><strong>Medication safety:<\/strong> Verify drug names, doses, changes, and allergies.<\/p>\n<\/li>\n<li>\n<p><strong>Traceability:<\/strong> Let reviewers inspect supporting context rather than relying on an unexplained confidence score.<\/p>\n<\/li>\n<li>\n<p><strong>Escalation:<\/strong> Provide a clear rejection and incident-reporting route.<\/p>\n<\/li>\n<\/ul>\n<p>Slice evaluation by specialty, language, acuity and patient demographic groups where lawful and appropriate. A global average can hide a failure concentrated in interpreted visits or a particular clinical template.<\/p>\n<h3>Measure supervision as work<\/h3>\n<p>Record review minutes, edits per note, and full-draft rejection rate. Define an edit consistently, distinguish stylistic changes from clinical corrections, and count rejection when the clinician abandons the draft rather than repairing it.<\/p>\n<p>A <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/40306686\/\" target=\"_blank\" rel=\"noopener\">2025 systematic review<\/a> found improvements in at least one efficiency measure in 9 of 10 studies, alongside variable accuracy, frequent manual editing, and inconsistent adoption. Faster drafting therefore doesn&#8217;t establish a lighter total workload.<\/p>\n<blockquote>\n<p>Count the time clinicians spend checking the machine, not just the time the machine spends writing.<\/p>\n<\/blockquote>\n<p>Use <a href=\"https:\/\/www.bridge-global.com\/services\/software-quality-assurance\">software quality assurance<\/a> for regression testing after model, prompt, template, or context-pipeline changes. Keep documentation production time separate from AI-management time, including escalation and audit work.<\/p>\n<h2>Privacy and Device Rules for Documentation AI<\/h2>\n<p>This is regulatory orientation, not legal advice. Build a jurisdiction-specific decision record with counsel rather than assuming that clinician review, regional hosting, or a vendor&#8217;s compliance statement resolves every obligation.<\/p>\n<p>For US deployments, have counsel map HIPAA applicability across audio, transcripts, prompts, and support access. Translate that review into access controls, minimum-necessary data flows, appropriate business-associate terms, incident handling and auditable operations.<\/p>\n<p>The <a href=\"https:\/\/healthit.gov\/regulations\/hti-rules\/hti-1-final-rule\/\" target=\"_blank\" rel=\"noopener\">ONC HTI-1 Final Rule<\/a> establishes transparency requirements for predictive algorithms incorporated into certified health IT, including source-attribute information, feedback mechanisms and risk-management practices. Determine whether the particular intervention falls within scope, then maintain versioned model information and ongoing review accordingly.<\/p>\n<h3>Match legal questions to engineering controls<\/h3>\n<ul>\n<li>\n<p><strong>GDPR:<\/strong> Document the lawful basis, processing purpose, retention, rights-handling and international-transfer position. For Netherlands deployments, include applicable Autoriteit Persoonsgegevens guidance in counsel&#8217;s review.<\/p>\n<\/li>\n<li>\n<p><strong>Device status:<\/strong> Obtain a written assessment of intended purpose under the relevant medical-device regime, including whether software as a medical device, or SaMD, questions arise.<\/p>\n<\/li>\n<li>\n<p><strong>EU AI Act:<\/strong> Assess the applicable medical-device and Annex III pathways rather than labelling all documentation software high-risk or exempt.<\/p>\n<\/li>\n<\/ul>\n<p>Mandatory clinician review isn&#8217;t a substitute for that classification assessment. Product claims about diagnosis or treatment should match the documented intended purpose.<\/p>\n<p>Our <a href=\"https:\/\/www.bridge-global.com\/blog\/hipaa-compliant-software-development\/\">HIPAA-compliant software development guide<\/a> provides implementation context. For patient-facing language, Guiding Growth&#8217;s <a href=\"https:\/\/guidinggrowth.app\/hipaa-compliant-app\/\" target=\"_blank\" rel=\"noopener\">parent&#8217;s guide to autism data privacy<\/a> offers a useful companion perspective, not a legal authority.<\/p>\n<p>We conduct GDPR and HIPAA gap analyses, implement necessary controls, and provide ongoing monitoring. The practical output should be an owned control register, not an unqualified compliance badge.<\/p>\n<h2>Rollout Metrics That Justify Scale<\/h2>\n<p>Start with a bounded pilot and a named clinical owner. Use <a href=\"https:\/\/www.bridge-global.com\/blog\/healthcare-workflow-optimization-software\/\">healthcare workflow optimization<\/a> to remove unnecessary steps before automating them.<\/p>\n<ul>\n<li>\n<p><strong>Define scope:<\/strong> Select a specialty, encounter type, and EHR note workflow.<\/p>\n<\/li>\n<li>\n<p><strong>Prepare participants:<\/strong> Train reviewers and obtain patient opt-in through a clear, scripted disclosure.<\/p>\n<\/li>\n<li>\n<p><strong>Baseline outcomes:<\/strong> Measure documentation time per encounter, after-hours note time, quality against a shared rubric, and clinician satisfaction.<\/p>\n<\/li>\n<li>\n<p><strong>Track supervision:<\/strong> Include clinical edits, full rejections, and review time.<\/p>\n<\/li>\n<li>\n<p><strong>Measure reach:<\/strong> Report adoption against eligible encounters, segmented by language, acuity, and clinician.<\/p>\n<\/li>\n<\/ul>\n<p>A <a href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC13154711\/\" target=\"_blank\" rel=\"noopener\">2026 emergency-medicine review<\/a> describes an academic ED study where ambient documentation was associated with a 28% reduction in on-shift documentation time, but adoption covered only 11.2% of eligible encounters. Don&#8217;t present results from selected users and visits as department-wide capacity gains.<\/p>\n<p>Stop expansion when severe errors or correction work make the workflow unacceptable, even if draft generation is fast. Redesign and revalidate before testing another specialty or acuity band.<\/p>\n<p>Bridge Global&#8217;s approach to <a href=\"https:\/\/www.bridge-global.com\/healthcare\">custom healthcare software development<\/a> includes readiness assessments, architecture guidance, resourcing plans, and compliance inputs. Our AI framework begins with discovery to assess readiness, define opportunities, and build a roadmap, giving the pilot an engineering plan before implementation begins.<\/p>\n<h2>Choosing the Right Documentation Tool With Confidence<\/h2>\n<p>Choose the sourcing path by assigning ownership of clinical risk. Then reject candidates that can&#8217;t substantiate specialty fit, reliable write-back, usable latency, transparent data handling, and workable consent.<\/p>\n<p>The strongest buying test isn&#8217;t fluent output. It&#8217;s a clinician completing a real encounter, correcting the draft inside the chart and signing with less total effort and acceptable residual risk.<\/p>\n<h3>Make the decision on operating evidence<\/h3>\n<p>Require a reproducible evaluation set, an owned safety process, and a written regulatory position. Keep commercial assumptions separate from measured clinical outcomes, particularly when forecasting capacity or financial return.<\/p>\n<p>Approve expansion only when the benefit survives the ordinary encounter mix, including patients who decline recording and clinicians who don&#8217;t become enthusiastic users. A tool that works only for selected visits may still have value, but its deployment scope should reflect that limitation.<\/p>\n<p>The right documentation layer makes the responsible clinician&#8217;s work easier to verify and complete. If supervision becomes heavier than authorship, change the workflow or the tool rather than scaling the problem.<\/p>\n<h2>Frequently Asked Questions<\/h2>\n<h3>What does AI clinical documentation include?<\/h3>\n<p>It includes ambient scribing, structured note drafts, coding suggestions, and encounter summaries. Each output needs a specific acceptance test and appropriate clinician review before use in the record or patient communication.<\/p>\n<h3>Should AI notes file into the EHR automatically?<\/h3>\n<p>Drafts can enter an explicitly provisional workspace, but they shouldn&#8217;t automatically become signed clinical content. Preserve the distinction between generated text, clinician corrections, and the approved record.<\/p>\n<h3>How should patients consent to ambient documentation?<\/h3>\n<p>Explain AI use, recording, storage, and who can access the transcript, with a visible recording indicator. Offer a non-recorded workflow without penalizing the patient and log the decision.<\/p>\n<h3>Which standard should carry the signed note?<\/h3>\n<p>Evaluate the EHR vendor&#8217;s supported API or a FHIR document workflow, including <code>DocumentReference<\/code> where appropriate. Confirm that authorship, timestamps, and provenance survive the transfer, and test how the receiving chart handles edits and signatures.<\/p>\n<h3>When is an AI documentation pilot ready to scale?<\/h3>\n<p>Scale when documentation time, note quality, review burden, clinician satisfaction and adoption meet the agreed acceptance criteria. Evaluate the actual encounter mix rather than relying on enthusiastic users or uncomplicated visits.<\/p>\n<hr \/>\n<p>We offer readiness assessment, architecture guidance, and healthcare software engineering to connect documentation drafting with consent, clinician review, and EHR integration. Visit <a href=\"https:\/\/www.bridge-global.com\">Bridge Global<\/a> to discuss a bounded pilot with explicit safety gates, write-back acceptance tests, and measurable supervision workload.<\/p><!-- AddThis Advanced Settings generic via filter on the_content --><!-- AddThis Share Buttons generic via filter on the_content -->","protected":false},"excerpt":{"rendered":"<p>AI clinical documentation turns encounter information into draft clinical content, and healthtech product teams should evaluate its accuracy, review burden, and fit with the EHR workflow. AI clinical documentation turns encounter information into draft notes, code suggestions, or summaries for &hellip;<!-- AddThis Advanced Settings generic via filter on get_the_excerpt --><!-- AddThis Share Buttons generic via filter on get_the_excerpt --><\/p>\n","protected":false},"author":224,"featured_media":58453,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1015],"tags":[1216,1841,2046,2047,2048],"class_list":["post-58454","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-healthcare","tag-ehr-integration","tag-ai-clinical-documentation","tag-ambient-scribe","tag-clinical-ai-safety","tag-hipaa-documentation"],"featured_image_src":"https:\/\/www.bridge-global.com\/blog\/wp-content\/uploads\/2026\/11\/ai-clinical-documentation-medical-consultation.jpg","author_info":{"display_name":"Stephanie Cornelissen","author_link":"https:\/\/www.bridge-global.com\/blog\/author\/stephanie\/"},"_links":{"self":[{"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/posts\/58454","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/users\/224"}],"replies":[{"embeddable":true,"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/comments?post=58454"}],"version-history":[{"count":2,"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/posts\/58454\/revisions"}],"predecessor-version":[{"id":58474,"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/posts\/58454\/revisions\/58474"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/media\/58453"}],"wp:attachment":[{"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/media?parent=58454"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/categories?post=58454"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.bridge-global.com\/blog\/wp-json\/wp\/v2\/tags?post=58454"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}